[et_pb_section bb_built=”1″ fullwidth=”on” _builder_version=”4.0.3″ next_background_color=”#000000″][et_pb_fullwidth_header title=”Publications” _builder_version=”4.0.3″ title_text_align=”center” title_font_size=”36px” background_image=”http://sites.bc.edu/amir-hoveyda/wp-content/uploads/sites/145/2019/12/header-5.jpg” /][/et_pb_section]
[et_pb_section bb_built=”1″ module_id=”research” _builder_version=”4.0.3″ prev_background_color=”#000000″ next_background_color=”#000000″][et_pb_row _builder_version=”4.0.3″ min_height=”369px” custom_margin=”-30px|||auto|false|false”][et_pb_column type=”4_4″ _builder_version=”4.0.3″][et_pb_text _builder_version=”4.10.5″ header_3_text_color=”#e02b20″ custom_padding=”||0px|||”]RESEARCH PUBLICATIONS
Review articles and patents are listed below separately.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.10.5″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.10.5″ header_3_text_color=”#e02b20″ custom_padding=”||0px|||” link_option_url=”doi.org/10.1021/jacs.1c11453″ hover_enabled=”0″ sticky_enabled=”0″ text_text_shadow_horizontal_length=”text_text_shadow_style,%91object Object%93″ text_text_shadow_horizontal_length_tablet=”0px” text_text_shadow_vertical_length=”text_text_shadow_style,%91object Object%93″ text_text_shadow_vertical_length_tablet=”0px” text_text_shadow_blur_strength=”text_text_shadow_style,%91object Object%93″ text_text_shadow_blur_strength_tablet=”1px” link_text_shadow_horizontal_length=”link_text_shadow_style,%91object Object%93″ link_text_shadow_horizontal_length_tablet=”0px” link_text_shadow_vertical_length=”link_text_shadow_style,%91object Object%93″ link_text_shadow_vertical_length_tablet=”0px” link_text_shadow_blur_strength=”link_text_shadow_style,%91object Object%93″ link_text_shadow_blur_strength_tablet=”1px” ul_text_shadow_horizontal_length=”ul_text_shadow_style,%91object Object%93″ ul_text_shadow_horizontal_length_tablet=”0px” ul_text_shadow_vertical_length=”ul_text_shadow_style,%91object Object%93″ ul_text_shadow_vertical_length_tablet=”0px” ul_text_shadow_blur_strength=”ul_text_shadow_style,%91object Object%93″ ul_text_shadow_blur_strength_tablet=”1px” ol_text_shadow_horizontal_length=”ol_text_shadow_style,%91object Object%93″ ol_text_shadow_horizontal_length_tablet=”0px” ol_text_shadow_vertical_length=”ol_text_shadow_style,%91object Object%93″ ol_text_shadow_vertical_length_tablet=”0px” ol_text_shadow_blur_strength=”ol_text_shadow_style,%91object Object%93″ ol_text_shadow_blur_strength_tablet=”1px” quote_text_shadow_horizontal_length=”quote_text_shadow_style,%91object Object%93″ quote_text_shadow_horizontal_length_tablet=”0px” quote_text_shadow_vertical_length=”quote_text_shadow_style,%91object Object%93″ quote_text_shadow_vertical_length_tablet=”0px” quote_text_shadow_blur_strength=”quote_text_shadow_style,%91object Object%93″ quote_text_shadow_blur_strength_tablet=”1px” header_text_shadow_horizontal_length=”header_text_shadow_style,%91object Object%93″ header_text_shadow_horizontal_length_tablet=”0px” header_text_shadow_vertical_length=”header_text_shadow_style,%91object Object%93″ header_text_shadow_vertical_length_tablet=”0px” header_text_shadow_blur_strength=”header_text_shadow_style,%91object Object%93″ header_text_shadow_blur_strength_tablet=”1px” header_2_text_shadow_horizontal_length=”header_2_text_shadow_style,%91object Object%93″ header_2_text_shadow_horizontal_length_tablet=”0px” header_2_text_shadow_vertical_length=”header_2_text_shadow_style,%91object Object%93″ header_2_text_shadow_vertical_length_tablet=”0px” header_2_text_shadow_blur_strength=”header_2_text_shadow_style,%91object Object%93″ header_2_text_shadow_blur_strength_tablet=”1px” header_3_text_shadow_horizontal_length=”header_3_text_shadow_style,%91object Object%93″ header_3_text_shadow_horizontal_length_tablet=”0px” header_3_text_shadow_vertical_length=”header_3_text_shadow_style,%91object Object%93″ header_3_text_shadow_vertical_length_tablet=”0px” header_3_text_shadow_blur_strength=”header_3_text_shadow_style,%91object Object%93″ header_3_text_shadow_blur_strength_tablet=”1px” header_4_text_shadow_horizontal_length=”header_4_text_shadow_style,%91object Object%93″ header_4_text_shadow_horizontal_length_tablet=”0px” header_4_text_shadow_vertical_length=”header_4_text_shadow_style,%91object Object%93″ header_4_text_shadow_vertical_length_tablet=”0px” header_4_text_shadow_blur_strength=”header_4_text_shadow_style,%91object Object%93″ header_4_text_shadow_blur_strength_tablet=”1px” header_5_text_shadow_horizontal_length=”header_5_text_shadow_style,%91object Object%93″ header_5_text_shadow_horizontal_length_tablet=”0px” header_5_text_shadow_vertical_length=”header_5_text_shadow_style,%91object Object%93″ header_5_text_shadow_vertical_length_tablet=”0px” header_5_text_shadow_blur_strength=”header_5_text_shadow_style,%91object Object%93″ header_5_text_shadow_blur_strength_tablet=”1px” header_6_text_shadow_horizontal_length=”header_6_text_shadow_style,%91object Object%93″ header_6_text_shadow_horizontal_length_tablet=”0px” header_6_text_shadow_vertical_length=”header_6_text_shadow_style,%91object Object%93″ header_6_text_shadow_vertical_length_tablet=”0px” header_6_text_shadow_blur_strength=”header_6_text_shadow_style,%91object Object%93″ header_6_text_shadow_blur_strength_tablet=”1px” box_shadow_horizontal_tablet=”0px” box_shadow_vertical_tablet=”0px” box_shadow_blur_tablet=”40px” box_shadow_spread_tablet=”0px” vertical_offset_tablet=”0″ horizontal_offset_tablet=”0″ z_index_tablet=”0″] 272. “E- and Z-trisubstituted macrocyclic alkenes for natural product synthesis and skeletal editing” Y. Mu, F. W. W. Hartrampf, E. C. Yu, K. E. Lounsbury, R. R. Schrock, F. Romiti, A. H. Hoveyda Nat. Chem. 2022. [/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.6.0″ header_3_text_color=”#e02b20″ custom_padding=”||0px|||” link_option_url=”https://www.nature.com/articles/s41557-022-00893-5“] 271. “Stereodefined Alkenes with a Fluoro-chloro Terminus as a Uniquely Enabling Compound Class” Q. Liu, Y. Mu, T. Koengeter, R. R. Schrock, A. H. Hoveyda Nat. Chem. 2022, 14, 463. [/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.6.0″ header_3_text_color=”#e02b20″ custom_padding=”||0px|||” link_option_url=”https://doi.org/10.1038/s41557-022-00893-5“] 270. “Cross-metathesis of Allenes. Mechanistic Analysis and Identification of a Ru-CAAC as the Most Effective Catalyst” S. A. Gonsales, Z. C. Mueller, F. Zhao, P. H. S. Paioti, L. Karmazin, J. Wan, F. Liu, K. N. Houk, A. H. Hoveyda J. Am. Chem. Soc. 2021, 143, 20640. [/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.10.5″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.10.5″ header_3_text_color=”#e02b20″ custom_padding=”||0px|||” link_option_url=”doi.org/10.1021/acs.organomet.1c00086″ hover_enabled=”0″ sticky_enabled=”0″ text_text_shadow_horizontal_length=”text_text_shadow_style,%91object Object%93″ text_text_shadow_horizontal_length_tablet=”0px” text_text_shadow_vertical_length=”text_text_shadow_style,%91object Object%93″ text_text_shadow_vertical_length_tablet=”0px” text_text_shadow_blur_strength=”text_text_shadow_style,%91object Object%93″ text_text_shadow_blur_strength_tablet=”1px” link_text_shadow_horizontal_length=”link_text_shadow_style,%91object Object%93″ link_text_shadow_horizontal_length_tablet=”0px” link_text_shadow_vertical_length=”link_text_shadow_style,%91object Object%93″ link_text_shadow_vertical_length_tablet=”0px” link_text_shadow_blur_strength=”link_text_shadow_style,%91object Object%93″ link_text_shadow_blur_strength_tablet=”1px” ul_text_shadow_horizontal_length=”ul_text_shadow_style,%91object Object%93″ ul_text_shadow_horizontal_length_tablet=”0px” ul_text_shadow_vertical_length=”ul_text_shadow_style,%91object Object%93″ ul_text_shadow_vertical_length_tablet=”0px” ul_text_shadow_blur_strength=”ul_text_shadow_style,%91object Object%93″ ul_text_shadow_blur_strength_tablet=”1px” ol_text_shadow_horizontal_length=”ol_text_shadow_style,%91object Object%93″ ol_text_shadow_horizontal_length_tablet=”0px” ol_text_shadow_vertical_length=”ol_text_shadow_style,%91object Object%93″ ol_text_shadow_vertical_length_tablet=”0px” ol_text_shadow_blur_strength=”ol_text_shadow_style,%91object Object%93″ ol_text_shadow_blur_strength_tablet=”1px” quote_text_shadow_horizontal_length=”quote_text_shadow_style,%91object Object%93″ quote_text_shadow_horizontal_length_tablet=”0px” quote_text_shadow_vertical_length=”quote_text_shadow_style,%91object Object%93″ quote_text_shadow_vertical_length_tablet=”0px” quote_text_shadow_blur_strength=”quote_text_shadow_style,%91object Object%93″ quote_text_shadow_blur_strength_tablet=”1px” header_text_shadow_horizontal_length=”header_text_shadow_style,%91object Object%93″ header_text_shadow_horizontal_length_tablet=”0px” header_text_shadow_vertical_length=”header_text_shadow_style,%91object Object%93″ header_text_shadow_vertical_length_tablet=”0px” header_text_shadow_blur_strength=”header_text_shadow_style,%91object Object%93″ header_text_shadow_blur_strength_tablet=”1px” header_2_text_shadow_horizontal_length=”header_2_text_shadow_style,%91object Object%93″ header_2_text_shadow_horizontal_length_tablet=”0px” header_2_text_shadow_vertical_length=”header_2_text_shadow_style,%91object Object%93″ header_2_text_shadow_vertical_length_tablet=”0px” header_2_text_shadow_blur_strength=”header_2_text_shadow_style,%91object Object%93″ header_2_text_shadow_blur_strength_tablet=”1px” header_3_text_shadow_horizontal_length=”header_3_text_shadow_style,%91object Object%93″ header_3_text_shadow_horizontal_length_tablet=”0px” header_3_text_shadow_vertical_length=”header_3_text_shadow_style,%91object Object%93″ header_3_text_shadow_vertical_length_tablet=”0px” header_3_text_shadow_blur_strength=”header_3_text_shadow_style,%91object Object%93″ header_3_text_shadow_blur_strength_tablet=”1px” header_4_text_shadow_horizontal_length=”header_4_text_shadow_style,%91object Object%93″ header_4_text_shadow_horizontal_length_tablet=”0px” header_4_text_shadow_vertical_length=”header_4_text_shadow_style,%91object Object%93″ header_4_text_shadow_vertical_length_tablet=”0px” header_4_text_shadow_blur_strength=”header_4_text_shadow_style,%91object Object%93″ header_4_text_shadow_blur_strength_tablet=”1px” header_5_text_shadow_horizontal_length=”header_5_text_shadow_style,%91object Object%93″ header_5_text_shadow_horizontal_length_tablet=”0px” header_5_text_shadow_vertical_length=”header_5_text_shadow_style,%91object Object%93″ header_5_text_shadow_vertical_length_tablet=”0px” header_5_text_shadow_blur_strength=”header_5_text_shadow_style,%91object Object%93″ header_5_text_shadow_blur_strength_tablet=”1px” header_6_text_shadow_horizontal_length=”header_6_text_shadow_style,%91object Object%93″ header_6_text_shadow_horizontal_length_tablet=”0px” header_6_text_shadow_vertical_length=”header_6_text_shadow_style,%91object Object%93″ header_6_text_shadow_vertical_length_tablet=”0px” header_6_text_shadow_blur_strength=”header_6_text_shadow_style,%91object Object%93″ header_6_text_shadow_blur_strength_tablet=”1px” box_shadow_horizontal_tablet=”0px” box_shadow_vertical_tablet=”0px” box_shadow_blur_tablet=”40px” box_shadow_spread_tablet=”0px” vertical_offset_tablet=”0″ horizontal_offset_tablet=”0″ z_index_tablet=”0″] 269. “Oxo 2-Adamantylidene Complexes of Mo(VI) and W(VI)” M. Boudjelel, F. Zhai, R. R. Schrock, A. H. Hoveyda, C. Tsay Organometallics 2021, 40, 838. [/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.10.5″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.10.5″ header_3_text_color=”#e02b20″ custom_padding=”||0px|||” link_option_url=”doi.org/10.1021/acs.inorgchem.0c03173″ hover_enabled=”0″ sticky_enabled=”0″ text_text_shadow_horizontal_length=”text_text_shadow_style,%91object Object%93″ text_text_shadow_horizontal_length_tablet=”0px” text_text_shadow_vertical_length=”text_text_shadow_style,%91object Object%93″ text_text_shadow_vertical_length_tablet=”0px” text_text_shadow_blur_strength=”text_text_shadow_style,%91object Object%93″ text_text_shadow_blur_strength_tablet=”1px” link_text_shadow_horizontal_length=”link_text_shadow_style,%91object Object%93″ link_text_shadow_horizontal_length_tablet=”0px” link_text_shadow_vertical_length=”link_text_shadow_style,%91object Object%93″ link_text_shadow_vertical_length_tablet=”0px” link_text_shadow_blur_strength=”link_text_shadow_style,%91object Object%93″ link_text_shadow_blur_strength_tablet=”1px” ul_text_shadow_horizontal_length=”ul_text_shadow_style,%91object Object%93″ ul_text_shadow_horizontal_length_tablet=”0px” ul_text_shadow_vertical_length=”ul_text_shadow_style,%91object Object%93″ ul_text_shadow_vertical_length_tablet=”0px” ul_text_shadow_blur_strength=”ul_text_shadow_style,%91object Object%93″ ul_text_shadow_blur_strength_tablet=”1px” ol_text_shadow_horizontal_length=”ol_text_shadow_style,%91object Object%93″ ol_text_shadow_horizontal_length_tablet=”0px” ol_text_shadow_vertical_length=”ol_text_shadow_style,%91object Object%93″ ol_text_shadow_vertical_length_tablet=”0px” ol_text_shadow_blur_strength=”ol_text_shadow_style,%91object Object%93″ ol_text_shadow_blur_strength_tablet=”1px” quote_text_shadow_horizontal_length=”quote_text_shadow_style,%91object Object%93″ quote_text_shadow_horizontal_length_tablet=”0px” quote_text_shadow_vertical_length=”quote_text_shadow_style,%91object Object%93″ quote_text_shadow_vertical_length_tablet=”0px” quote_text_shadow_blur_strength=”quote_text_shadow_style,%91object Object%93″ quote_text_shadow_blur_strength_tablet=”1px” header_text_shadow_horizontal_length=”header_text_shadow_style,%91object Object%93″ header_text_shadow_horizontal_length_tablet=”0px” header_text_shadow_vertical_length=”header_text_shadow_style,%91object Object%93″ header_text_shadow_vertical_length_tablet=”0px” header_text_shadow_blur_strength=”header_text_shadow_style,%91object Object%93″ header_text_shadow_blur_strength_tablet=”1px” header_2_text_shadow_horizontal_length=”header_2_text_shadow_style,%91object Object%93″ header_2_text_shadow_horizontal_length_tablet=”0px” header_2_text_shadow_vertical_length=”header_2_text_shadow_style,%91object Object%93″ header_2_text_shadow_vertical_length_tablet=”0px” header_2_text_shadow_blur_strength=”header_2_text_shadow_style,%91object Object%93″ header_2_text_shadow_blur_strength_tablet=”1px” header_3_text_shadow_horizontal_length=”header_3_text_shadow_style,%91object Object%93″ header_3_text_shadow_horizontal_length_tablet=”0px” header_3_text_shadow_vertical_length=”header_3_text_shadow_style,%91object Object%93″ header_3_text_shadow_vertical_length_tablet=”0px” header_3_text_shadow_blur_strength=”header_3_text_shadow_style,%91object Object%93″ header_3_text_shadow_blur_strength_tablet=”1px” header_4_text_shadow_horizontal_length=”header_4_text_shadow_style,%91object Object%93″ header_4_text_shadow_horizontal_length_tablet=”0px” header_4_text_shadow_vertical_length=”header_4_text_shadow_style,%91object Object%93″ header_4_text_shadow_vertical_length_tablet=”0px” header_4_text_shadow_blur_strength=”header_4_text_shadow_style,%91object Object%93″ header_4_text_shadow_blur_strength_tablet=”1px” header_5_text_shadow_horizontal_length=”header_5_text_shadow_style,%91object Object%93″ header_5_text_shadow_horizontal_length_tablet=”0px” header_5_text_shadow_vertical_length=”header_5_text_shadow_style,%91object Object%93″ header_5_text_shadow_vertical_length_tablet=”0px” header_5_text_shadow_blur_strength=”header_5_text_shadow_style,%91object Object%93″ header_5_text_shadow_blur_strength_tablet=”1px” header_6_text_shadow_horizontal_length=”header_6_text_shadow_style,%91object Object%93″ header_6_text_shadow_horizontal_length_tablet=”0px” header_6_text_shadow_vertical_length=”header_6_text_shadow_style,%91object Object%93″ header_6_text_shadow_vertical_length_tablet=”0px” header_6_text_shadow_blur_strength=”header_6_text_shadow_style,%91object Object%93″ header_6_text_shadow_blur_strength_tablet=”1px” box_shadow_horizontal_tablet=”0px” box_shadow_vertical_tablet=”0px” box_shadow_blur_tablet=”40px” box_shadow_spread_tablet=”0px” vertical_offset_tablet=”0″ horizontal_offset_tablet=”0″ z_index_tablet=”0″] 268. “Boosting the Metathesis Activity of Molybdenum Oxo Alkylidenes by Tuning the Anionic Ligand σ Donation” J. De Jesus Silva, M. Pucino, F. Zhai, D. Mance, Z. J. Berkson, D. F. Nater, A. H. Hoveyda, C. Copéret, R. R. Schrock Inorg. Chem. 2021, 60, 6875. [/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.6.0″ header_3_text_color=”#e02b20″ custom_padding=”||0px|||” link_option_url=”https://pubs.acs.org/doi/10.1021/acs.organomet.0c00275″] 267. “Streamlined Catalytic Enantioselective Synthesis of α-Substituted β,γ-Unsaturated Ketones and Either of the Corresponding Tertiary Homoallylic Alcohol Diastereomers” J. del Pozo, S. Zhang, F. Romiti, S. Xu, R. P. Conger, A. H. Hoveyda J. Am. Chem. Soc. 2020, 142, 18200. [/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.5.1″ header_3_text_color=”#e02b20″ custom_padding=”||0px|||” link_option_url=”https://pubs.acs.org/doi/10.1021/acs.organomet.0c00275″]266. “Syntheses of “Phosphine-Free” Molybdenum Oxo Alkylidene Complexes through Addition of Water to Alkylidyne Complexes” F. Zhai, R. R. Schrock, A. H. Hoveyda, P. Müller Organometallics 2020, 39, 2486.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.6.0″ header_3_text_color=”#e02b20″ custom_padding=”||0px|||” link_option_url=”https://doi.org/10.1002/anie.202003755″]265. “Sulfonate N‐Heterocyclic Carbene–Copper Complexes: Uniquely Effective Catalysts for Enantioselective Synthesis of C−C, C−B, C−H, and C−Si Bonds” A. H. Hoveyda, Y. Zhou, Y. Shi, M. K. Brown, H. Wu, S. Torker Angew. Chem., Int. Ed. 2020, 59, 21304.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.6.0″ header_3_text_color=”#e02b20″ custom_padding=”||0px|||” link_option_url=”https://doi.org/10.1002/anie.202001184″]264. “Regio‐ and Enantioselective Synthesis of Trifluoromethyl‐Substituted Homoallylic α‐Tertiary NH2‐Amines by Reactions Facilitated by a Threonine‐Based Boron‐Containing Catalyst” D. C. Fager, R. J. Morrison, A. H. Hoveyda Angew. Chem., Int. Ed. 2020, 59, 11448.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.11″ header_3_text_color=”#e02b20″ custom_padding=”||0px|||” link_option_url=”https://doi.org/10.1021/jacs.9b11178″]263. “A Catalytic Approach for Enantioselective Synthesis of Homoallylic Alcohols Bearing Z-Alkenyl Chloride or Trifluoromethyl Group. A Protecting Group-Free Synthesis of Mycothiazole” R. J. Morrison, F. W. van der Mei, F. Romiti, A. H. Hoveyda J. Am. Chem. Soc. 2020, 142, 436.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.11″ header_3_text_color=”#e02b20″ custom_padding=”||0px|||”]262. “Catalytic Enantioselective Conjugate Addition of Stereodefined Di- and Trisubstituted Alkenylaluminum Compounds to Acyclic Enones” K. P. McGrath, A. K. Hubbell, Y. Zhou, D. P.Santos, S. Torker, F. Romiti, A. H. Hoveyda Adv. Synth. Catal. 2020, 362, 370. (Special issue dedicated to the sixtieth birthday of Professor Eric N. Jacobsen)
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.11″ header_3_text_color=”#e02b20″ custom_padding=”||0px|||”]261. “Catalytic Enantioselective Boryl and Silyl Substitution with Trifluoromethyl Alkenes: Scope, Utility, and Mechanistic Nuances of Cu−F β‑Elimination” P. H. S. Paioti, J. del Pozo, M. S. Mikus, J. Lee, M. J. Koh, F. Romiti, S. Torker, A. H. Hoveyda J. Am. Chem. Soc. 2019, 141, 19917.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″ header_3_text_color=”#e02b20″ custom_padding=”||0px|||”]260. “Catalytic Enantioselective Addition of an Allyl Group to Ketones Containing a Tri-, a Di-, or a Monohalomethyl Moiety. Stereochemical Control Based on Distinctive Electronic and Steric Attributes of C–Cl, C–Br, and C–F Bonds” D. C. Fager, K. Lee, A. H. Hoveyda J. Am. Chem. Soc. 2019, 141, 16125.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]259. “Copper–Hydride-Catalyzed Enantioselective Processes with Allenyl Boronates. Mechanistic Nuances, Scope, and Utility in Target-Oriented Synthesis” Y. Sun, Y. Zhou, Y. Shi, J. del Pozo, S. Torker, A. H. Hoveyda J. Am. Chem. Soc. 2019, 141,12087.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]258. “Catalytic Enantioselective Synthesis of Allylic Boronates with a Trisubstituted Alkenyl Fluoride and Conversion to Compounds with a F-Substituted Stereogenic Quaternary Center” S. Akiyama, K. Kubota, M. S. Mikus, P. H. S. Paioti, F. Romiti, Q. Liu, Y. Zhou, A. H. Hoveyda, H. Ito Angew. Chem., Int. Ed. 2019, 58, 11998.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]257. “Silica‐Supported Molybdenum‐Oxo Alkylidenes: Bridging the Gap between Internal and Terminal Olefin Metathesis” M. Pucino, F. Zhai, C. P. Gordon, D. Mance, A. H. Hoveyda, R. R. Schrock, C. Copéret Angew. Chem., Int. Ed. 2019, 58, 11816.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]256. “Ru-Based Catechothiolate Complexes Bearing an Unstaturated NHC Ligand: Effective Cross-Metathesis Catalysts for Synthesis of (Z)-α,β-Unsaturated Esters, Caboxylic Acids and Primary, Secondary, and Weinreb Amides” Z. Liu, C. Xu, J. del Pozo, S. Torker, A. H. Hoveyda J. Am. Chem. Soc. 2019, 141, 7137.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]255. “E– and Z-, Di- and Tri-Substituted Alkenyl Nitriles Through Catalytic Cross-Metathesis” Y. Mu, T. Nguyen, M.J. Koh, R. R. Schrock, A. H. Hoveyda Nat. Chem. 2019, 11, 478.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]254. “Delayed Catalyst Function Enables Direct Enantioselective Conversion of Nitriles to NH2-Amines” S. Zhang, J. del Pozo, F. Romiti, Y. Mu, S. Torker, A. H. Hoveyda Science 2019, 364, 45.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]253. “Traceless Protection for More Broadly Applicable Olefin Metathesis” Y. Mu, T. Nguyen, F. W. van der Mei, R. R. Schrock, A. H. Hoveyda Angew. Chem., Int. Ed. 2019, 58, 5365.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]252. “Racemic Vinylallenes in Catalytic Enantioselective Mutlicomponent Processes. Rapid Generation of Complexity through 1,6-Conjugate Additions” Y. Huang, S. Torker, X. Li, J. del Pozo, A. H. Hoveyda Angew. Chem., Int. Ed. 2019, 58, 2685.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]251. “SN2″-Selective and Enantioselective Substitution with Unsaturated Organoboron Compounds and Catalyzed by a Sulfonate-Containing NHC-Cu Complex” Y. Zhou, Y. Shi, S. Torker, and A. H. Hoveyda J. Am. Chem. Soc. 2018, 140, 16842.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]250. “Syntheses of Molybendenum Oxo Benzylidene Complexes” F. Zhai, K. V. Bukhryakov, R.R. Schrock, A. H. Hoveyda, C. Tsay, P. Müller J. Am. Chem. Soc. 2018, 140, 13609.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]249. “γ-, Diastereo-, and Enantioselective Addition of MEMO-Substituted Allylboron Compounds to Aldimines Catalyzed by Organoboron-Ammonium Complexes” A. H. Hoveyda, R. J. Morrison Angew. Chem., Int. Ed. 2018, 57, 11654.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]248. “Syntheses of High-Oxidation-State Mo═CHX Complexes, Where X = Cl, CF3, Phosphonium, CN” S. VenkatRamani, R.R. Schrock, A. H. Hoveyda, P. Müller, C. Tsay Organometallics 2018, 37, 1641.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]247. “Syntheses of Molybendenum Oxo Alkylidene Complexes through Addition of Water to an Alkylidyne Complex” K. V. Bukhryakov, R.R. Schrock, A. H. Hoveyda, C. Tsay, P. Müller J. Am. Chem. Soc. 2018, 140, 2797.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]246. “Enantioselective Synthesis for Trisubstituted Allenyl—B(pin) Compounds by Phosphine—Cu-Catalyzed 1,3-Enyne Hydroboration. Insights Regarding Stereochemical Intergrity of Cu—Allenyl Intermediates” Y. Huang, J. del Pozo, S. Torker, A. H. Hoveyda J. Am. Chem. Soc. 2018, 140, 2643.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]245. “Mechanism-based Enhancement of Scope and Enantioselectivity for Reactions Involving a Copper-Substituted Stereogenic Carbon Centre” J. Lee, S. Radomkit, S. Torker, J. del Pozo, A. H. Hoveyda Nat. Chem. 2018, 10, 99.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]244. “Synthesis of E-and Z-Trisubstituted Alkenes by Catalytic Cross-Metathesis” T. T. Nguyen, M. J. Koh, T. J. Mann, R. R. Schrock, A. H. Hoveyda Nature 2017, 552, 347.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]243. “Synthesis of Z– or E-Trisubstituted Allylic Alcohols and Ethers by Kinetically Controlled Cross-Metathesis with a Ru Catechothiolate Complex” C. Xu, Z. Liu, S. Torker, X. Shen, D. Xu, A.H. Hoveyda J. Am. Chem. Soc. 2017, 139, 15640.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]242. “Synthesis of Molybdenum Adamantylimido and t-Butylimido Alkylidene Chloride Complexes Using HCl and Diphenylmenthylphosphine” K. V. Bukhryakov, S. VenkatRamani, C. Tsay, A. Hoveyda, R. R. Schrock Organometallics 2017, 36, 4208.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]241. “Enantioselective Total Synthesis of (—)-Deoxoapodine” T. Kang, K. L. White, T. J. Mann, A. H. Hoveyda, M. Movassaghi Angew. Chem., Int. Ed. 2017, 56, 13857.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]240. “In Situ Methylene Capping: A General Strategy for Efficient Stereoretentive Catalytic Olefin Metathesis. The Concept, Methodological Implications, and Applications to Synthesis of Biologically Active Compounds” C. Xu, X. Shen, A. H. Hoveyda J. Am. Chem. Soc. 2017, 139, 10919.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]239. “Catalytic Diastereo- and Enantioselective Additions of Versatile Allyl Groups to N-H Ketimines,“ H. Jang, F. Romiti, S. Torker, A. H. Hoveyda Nat. Chem. 2017, 9, 1269.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]238. “Practical, Broadly Applicable, α- Selective, Z-Selective, Diastereoselective and Enantioselective Addition of Allylboron Compounds to Mono-, Di-, Tri- and Polyfluoroalkyl Ketones,“ F. W. van der Mei, C. Qin, R. J. Morrison, A. H. Hoveyda J. Am. Chem. Soc. 2017, 139, 9053.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]237. “Practical, Efficient, and Broadly Applicable Synthesis of Readily Differentiable Vicinal Diboronate Compounds by Catalytic Three-Component Reactions,“ S. Radomkit, Z. Liu, A. Closs, M.S. Mikus, A. H. HoveydaTetrahedron, 2017, 73, 5011. (Special issue in honor of Professor Ben Feringa)
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]236. “Electronically Activated Organoboron Catalysts for Enantioselective Propargyl Addition to Trifluoromethyl Ketones,“ N.W. Mszar, M. S. Mikus, S. Torker, F. Haeffner, A. H. Hoveyda Angew. Chem., Int. Ed. 2017, 56, 8736.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]235. “Synthesis of 2,6,-Hexa-tert-butylterphenyl Derivatives, 2,6-(2,4,6-t-Bu3C6H2)2C6H3X, where X + I, Li, OH, SH, N3, or NH2,“ K.V. Bukhryakov, R. R. Schrock, A. H. Hoveyda, P. Müller, J. Becker Org. Lett. 2017, 19, 2607.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]234. “Molybdenum Chloride Catalysts for Z-Selective Olefin Metathesis Reactions,“ M. J. Koh, T. T. Nguyen, J. K. Lam, S. Torker, J. Hyvl, R. R. Schrock, A. H. Hoveyda Nature 2017, 542, 80.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]233. “Kinetically E-Selective Macrocyclic Ring-Closing Metathesis,“ X. Shen, T. T. Nguyen, M. J. Koh, D. Xu, A. W. H. Speed, R. R. Schrock, A. H. Hoveyda Nature 2017, 541, 380.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]232. “Versatile Homoallylic Boronates by Chemo-, SN2′-, Diastereo- and Enantioslective Catalytic Sequence of Cu—H Addition to Vinyl-B(pin)/Allylic Substitution,” J. Lee, S. Torker, A. H. Hoveyda Angew. Chem., Int. Ed. 2017, 56, 821.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]231. “Synthesis and Evaluation of Molybdenum and Tungsten Monoaryloxide Halide Alkylidene Complexes for Z-Selective Cross-Metathesis of Cyclooctene and Z-1,2-Dichloroethylene,” J. Lam, C. Zhu, K. V. Bukhryakov, P. Müller, A. H. Hoveyda, R. R. Schrock J. Am. Chem. Soc. 2016, 138, 15774.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]230. “Pentacoordinate Ruthenium(ll) Catecholthiolate and Mercaptophenolate Catalysts for Olefin Metathesis: Anionic Ligand Exchange and Ease of Initiation,” M. S. Mikus, S. Torker, C. Xu, B. Li, A. H. Hoveyda Organometallics 2016, 35, 3878.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]229. “Synthesis of Linear (Z)- α , β -Unsaturated Esters by Catalytic Crosss-Metathesis. The Influence of Acetonitrile,” E. C. Yu, B. M. Johnson, E. M. Townsend, R. R. Schrock, A. H. Hoveyda Angew. Chem., Int. Ed. 2016, 55, 13210.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]228. “Catalytic Enantioselective 1,6-Conjugate Additions of Propargyl and Allyl Groups,” F. Meng, X. Li, S. Torker, Y. Shi, X. Shen, A. H. Hoveyda Nature 2016, 537, 387.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]227. “Catalytic Enantioselective Conjugate Additions of (pin)B-Substituted Allylcopper Compounds Generated in situ from Butadiene or Isoprene,” X. Li, F. Meng, S. Torker, Y. Shi, A. H. Hoveyda Angew. Chem., Int. Ed. 2016, 55, 9997.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]226. “Practical and Broadly Applicable Catalytic Enantioselective Additions of Allyl–B(pin) Compounds to Ketones and α -Ketoesters,” D. W. Robbins, K. Lee, D. L. Silverio, A. Volkov, S. Torker, A. H. Hoveyda Angew. Chem., Int. Ed. 2016, 55, 9610.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]225. “Catalytic Enantioselective Addition of Organoboron Reagents to Fluoroketones Controlled by Electrostatic Interactions,” K. Lee, D. L. Silverio, S. Torker, F. Haeffner, D. W. Robbins, F. W. van der Mei, A. H. Hoveyda Nat. Chem. 2016, 8, 768.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]224. “Kinetically controlled E-Selective Catalytic Olefin Metathesis,” T. T. Nguyen, M. J. Koh, X. Shen, F. Romiti, R. R. Schrock, A. H. Hoveyda Science 2016, 352, 569.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]223. “Controllable ROMP Tacticity by Harnessing the Fluxionality of Stereogenic-at-Ruthenium Complexes,“ M. S. Mikus, S. Torker, A. H. Hoveyda Angew. Chem., Int. Ed. 2016, 55, 4997.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]222. “Lewis Acid Catalyzed Borotropic Shifts in the Design of Diastereo- and Enantioselective γ-Additions of Allylboron Moieties to Aldimines,” F. W. van der Mei, H. Miyamoto, D. L. Silverio, A. H. Hoveyda Angew. Chem., Int. Ed. 2016, 55, 4701.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]221. “Catalytic SN2′- and Enantioselective Allylic Substitution with a Diborylmethane Reagent and Application in Synthesis,” Y. Shi, A. H. Hoveyda Angew. Chem., Int. Ed. 2016, 55, 3455.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]220. “Direct Synthesis of Z-Alkenyl Halides through Catalytic Cross-Methathesis,” M. J. Koh, T. T. Nguyen, H. Zhang, R. R. Schrock, A. H. Hoveyda Nature 2016, 531, 459.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]219. “Regarding a Persisting Puzzle in Olefin Metathesis with Ru Complexes: Why are Transformations of Alkenes with a Small Substituent Z-Selective?,” S. Torker, M. J. Koh, R. K. Khan, A. H. Hoveyda Organometallics 2016, 35, 543.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]218. “Mechanism of NHC-Catalyzed Conjugate Additions of Diboron and Borosilane Reagents to β Unsaturated Carbonyl Compounds” H. Wu, J. M. Garcia, F. Haeffner, S. Radomkit, A. R. Zhugralin, A. H. Hoveyda J. Am. Chem. Soc. 2015, 137, 10585.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]217. “N-Heterocyclic Carbene–Copper-Catalyzed Group-, Site-, and Enantioselective Allylic Substitution with a Readily Accessible Propargyl(pinacolato)boron Reagent: Utility in Stereoselective Synthesis and Mechanistic Attributes,” Y. Shi , B. Jung , S. Torker, A. H. Hoveyda J. Am. Chem. Soc. 2015, 137, 8948.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]216. “N-Substituted Tertiary and O-Substituted Quaternary Carbon Stereogenic Centers by Site-, Diastereo- and Enantioselective Vinylogous Mannich Reactions,” D. L. Silverio, P. Fu, E. L. Carswell, M. L. Snapper, A. H. Hoveyda Tetrahedron Lett. 2015, 56, 3489. (Special issue in memory of Professor Harry H. Wasserman)
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]215. “Synthesis of Molybdenum and Tungsten Alkylidene Complexes that Contain the 2,6-Bis(2,4,6-triisopropylphenyl)phenylimido (NHIPT) Ligand,” J. C. Axtell, R. R. Schrock, Peter Müller, A. H. Hoveyda Organometallics 2015, 34, 2110.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]214. “Synthesis of Alternating trans-AB Copolymers through Ring-Opening Metathesis Polymerization Initiated by Molybdenum Alkylidenes,” H. Jeong, J. M. John, R. R. Schrock, A. H. HoveydaJ. Am. Chem. Soc. 2015, 137, 2239.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]213. “High-Value Alcohols and Higher-Oxidation-State Compounds by Catalytic Z-Selective Cross-Metathesis,” M. J. Koh, R. K. M. Khan, S. Torker, M. Yu, M. S. Mikus, A. H. Hoveyda Nature 2015, 517, 181.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]212. “Catalyst-Controlled Stereoselective Olefin Metathesis as a Principal Strategy in Multistep Synthesis Design: A Concise Route to (+)-Neopeltolide,” M. Yu, R. R. Schrock, A. H. Hoveyda Angew. Chem., Int. Ed. 2015, 54, 215.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]211. “Preparation of Macrocyclic Z-Enoates and (E,Z)- or (Z,E)-Dienoates through Catalytic Stereoselective Ring-Closing Metathesis,” H. Zhang, E. C. Yu, S. Torker, R. R. Schrock, A. H. Hoveyda J. Am. Chem. Soc. 2014, 136, 16493.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]210. “Catalytic Z-Selective Cross-Metathesis in Complex Molecule Synthesis: A Convergent Stereoselective Route to Disorazole C1,” A. W. H. Speed, T. J. Mann, R. V. O’Brien, R. R. Schrock, A. H. Hoveyda J. Am. Chem. Soc. 2014, 136, 16136.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]209. “Reactivity and Selectivity Differences between Catecholate and Catechothiolate Ru Complexes. Implications Regarding Design of Stereoselective Olefin Metathesis Catalysts,” R. K. M. Khan, S. Torker, A. H. Hoveyda J. Am. Chem. Soc. 2014, 136, 14337.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]208. “Synthesis of Molybdenum and Tungsten Alkylidene Complexes That Contain Sterically Demanding Arenethiolate Ligands,” E. M. Townsend, J. Hyvl, W. P. Forrest, R. R. Schrock, P. Müller, A. H. Hoveyda Organometallics 2014, 33, 5334.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]207. “Multifunctional Organoboron Compounds for Scalable Natural Product Synthesis,” F. Meng, K. P. McGrath, A. H. Hoveyda Nature 2014, 513, 367.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]206. “Synthesis of Tungsten Imido Alkylidene Complexes that Contain an Electron-Withdrawing Imido Ligand,” J. C. Axtell, R. R. Schrock, P. Müller, S. J. Smith, A. H. Hoveyda Organometallics 2014, 33, 5342.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]205. “Catalytic Enantioselective Protoboration of Disubstituted Allenes. Access to Alkenylboron Compounds in High Enantiomeric Purity,” H. Jang, B. Jung, A. H. Hoveyda Org. Lett. 2014, 16, 4658.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]204. “Diastereo- and Enantioselective Reactions of Bis(pinacolato)diboron, 1,3-Enynes, and Aldehydes Catalyzed by an Easily Accessible Bisphosphine–Cu Complex,” F. Meng, F. Haeffner, A. H. Hoveyda J. Am. Chem. Soc. 2014, 136, 11304.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]203. “Synthesis of (±)-Tetrapetalone A-Me Aglycon,” P. N. Carlsen, T. J. Mann, A. H. Hoveyda, A. J. Frontier Angew. Chem., Int. Ed. 2014, 53, 9334.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]202. “An Efficient, Practical, and Enantioselective Method for Synthesis of Homoallenylamides Catalyzed by an Aminoalcohol-Derived, Boron-Based Catalyst,” H. Wu, F. Haeffner, A. H. Hoveyda J. Am. Chem. Soc. 2014, 136, 3780.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]201. “NHC–Cu-Catalyzed Addition of Propargylboron Reagents to Phosphinoylimines. Enantioselective Synthesis of Trimethylsilyl-Substituted Homoallenylamides and Application to the Synthesis of S-(–)-Cyclooroidin,” N. W. Mszar, F. Haeffner, A. H. Hoveyda J. Am. Chem. Soc. 2014, 136, 3362.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]200. “The Influence of Anionic Ligands on Stereoisomerism of Ru Carbenes and Their Importance to Efficiency and Selectivity of Catalytic Olefin Metathesis Reactions,” S. Torker, R. K. M. Khan, A. H. Hoveyda J. Am. Chem. Soc. 2014, 136, 3439.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]199. “Enantioselective Synthesis of Boron-Substituted Quaternary Carbon Stereogenic Centers through NHC-Catalyzed Conjugate Additions of (Pinacolato)boron Units to Enones,” S. Radomkit, A. H. Hoveyda Angew. Chem., Int. Ed. 2014, 53, 3387.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]198. “A Broadly Applicable NHC–Cu-Catalyzed Approach for Efficient, Site-, and Enantioselective Coupling of Readily Accessible (Pinacolato)alkenylboron Compounds to Allylic Phosphates and Applications to Natural Product Synthesis,” F. Gao, J. L. Carr, A. H. Hoveyda J. Am. Chem. Soc. 2014, 136, 2149.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]197. “Broadly Applicable Z– and Diastereoselective Ring-Opening/Cross-Metathesis Catalyzed by a Dithiolate Ru Complex,” M. J. Koh, R. K. M. Khan, S. Torker, A. H. Hoveyda Angew. Chem., Int. Ed. 2014, 53, 1968.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]196. “A Multicomponent Ni-, Zr-, and Cu-Catalyzed Strategy for Enantioselective Synthesis of Alkenyl-Substituted Quaternary Carbons,” K. P. McGrath, A. H. Hoveyda Angew. Chem., Int. Ed. 2014, 53,1910.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]195. “High Oxidation State Molybdenum Imido Heteroatom-Substituted Alkylidene Complexes,” E. M. Townsend, S. M. Kilyanek, R. R. Schrock, P.Müller, S. J. Smith, A. H. Hoveyda Organometallics 2013, 32, 4612.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]194. “Enantioselective Silyl Protection of Alcohols Promoted by a Combination of Chiral and Achiral Lewis Basic Catalysts,” N. Mannville, H. Alite, F. Haeffner, A. H. Hoveyda, M. L. Snapper Nat. Chem. 2013, 5, 768.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]193. “Catalytic Z-Selective Cross-Metathesis with Secondary Silyl- and Benzyl-Protected Allylic Ethers: Mechanistic Aspects and Applications to Natural Product Synthesis,” T. J. Mann, A. W. H. Speed, R. R. Schrock, A. H. Hoveyda Angew. Chem., Int. Ed. 2013, 52, 8395.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]192. “Readily Accessible and Easily Modifiable Ru-Based Catalysts for Efficient and Z-Selective Ring-Opening Metathesis Polymerization and Ring-Opening/Cross-Metathesis,” R. K. M. Khan, S. Torker, A. H. Hoveyda J. Am. Chem. Soc. 2013, 135, 10258.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]191. “Enantioselective Synthesis of Quaternary Carbon Stereogenic Centers through Cu-Catalyzed Conjugate Additions of Aryl- and Alkylaluminum Reagents to Acyclic Trisubstituted Enones,” J. A. Dabrowski, M. T. Villaume, A. H. Hoveyda Angew. Chem., Int. Ed. 2013, 52, 8156.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]190. “Combining NHC–Cu and BØnsted Base Catalysis: Enantioselective Allylic Substitition/Conjugate Addition with Alkynyllithium Reagents and Stereospecific Isomerization of Products to Trisubstituted Allenes,” J. A. Dabrowski, J. Haeffner, A. H. Hoveyda Angew. Chem., Int. Ed. 2013, 52, 7694.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]189. “Synthesis of Z-(Pinacolato)allylboron and Z-(Pinacolato)alkenylboron Compounds through Stereoselective Catalytic Cross-Metathesis,” E. T. Kiesewetter, R. V. O’Brien, E. C. Yu, S. J. Meek, R. R. Schrock, A. H. Hoveyda J. Am. Chem. Soc. 2013, 135, 6026.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]188. “Cu-Catalyzed Chemoselective Preparation of 2-(Pinacolato)boron-Substituted Allylcopper Complexes and their In Situ Site-, Diastereo-, and Enantioselective Additions to Aldehydes and Ketones,” F. Meng, H. Jang, B. Jung, A. H. Hoveyda Angew. Chem., Int. Ed. 2013, 52, 5046.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]187. “NHC-Cu-Catalyzed Protoboration of Monosubstituted Allenes. Ligand-Controlled Site Selectivity, Application to Synthesis and Mechanism,” F. Meng, B. Jung, F. Haeffner, A. H. Hoveyda Org. Lett. 2013, 15, 1414.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]186. “Simple Organic Molecules as Catalysts for Enantioselective Synthesis of Amines and Alcohols,” D. Silverio, S. Torker, T. Pilyugina, E. M. Vieira, M. L. Snapper, F. Haeffner, A. H. Hoveyda Nature 2013, 494, 216.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]185. “Efficient and Selective Formation of Macrocyclic Disubstituted Z Alkenes by Ring-Closing Metathesis (RCM) Reactions Catalyzed by Mo- or W-Based Monoaryloxide Pyrrolide (MAP) Complexes: Applications to Total syntheses of Epilachnene, Yuzu Lactone, Ambrettolide, Epothilone C, and Nakadomarin A,” C. Wang, M. Yu, A. F. Kyle, P. Jakubec, D. J. Dixon, R. R. Schrock, A. H. Hoveyda Chem. Eur. J. 2013, 19, 2726.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]184. “Exceptionally E– and β-Selective NHC-Cu-Catalyzed Proto-Silyl Additions to Terminal Alkynes and Site- and Enantioselective Proto-Boryl Additions to the Resulting Vinylsilanes: Synthesis of Enantiomerically Enriched Vicinal and Geminal Borosilanes,” F. Meng, H. Jang, A. H. Hoveyda Chem. Eur. J. 2013, 19, 3204.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]183. “Molybdenum-Based Complexes with Two Aryloxides and a Pentafluoroimido Ligand: Catalysis for Efficient Z-selective Synthesis of a Macrocylic Trisubstituted Alkene by Ring Closing Metathesis,” C. Wang, F. Haeffner, R. R. Schrock, A. H. Hoveyda Angew. Chem., Int. Ed. 2013, 52, 1939.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]182. “NHC–Cu-Catalyzed Silyl Conjugate Additions to Acyclic and Cyclic Dienones and Dienoates. Efficient Site-, Diastereo- and Enantioselective Synthesis of Carbonyl-Containing Allylsilanes,” K.-S. Lee, H. Wu, F. Haeffner, A. H. Hoveyda Organometallics 2012, 31, 7823.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]181. “Z– and Enantioselective Ring-Opening/Cross-Metathesis with Enol Ethers Catalyzed by Stereogenic-at-Ru Carbenes: Reactivity, Selectivity, and Curtin-Hammett Kinetics,” R. K. M. Khan, R. V. O’Brien, S. Torker, B. Li, A. H. Hoveyda J. Am. Chem. Soc. 2012, 134, 12774.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]180. “Synthesis, Isolation, Characterization, and Reactivity of High-Energy Stereogenic-at-Ru Carbenes: Stereochemical Inversion through Olefin Metathesis and Other Pathways,” R. K. M. Khan, A. R. Zhugralin, S. Torker, R. V. O’Brien, P. J. Lombardi, A. H. Hoveyda J. Am. Chem. Soc. 2012, 134, 12438.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]179. “Z-selective Metathesis Homocoupling of 1,3-Dienes by Molybdenum and Tungsten Monoaryloxide Pyrrolide (MAP) Complexes,” E. M. Townsend, R. R. Schrock, A. H. Hoveyda J. Am. Chem. Soc. 2012, 134, 11334.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]178. “Bipyridine Adducts of Molybdenum Imido Alkylidene and Imido Alkylidyne Complexes,” A. G. Lichtscheidl, V. W. L. Ng, P. Müller, M. K. Takase, R. R. Schrock, S. J. Malcolmson, S. J. Meek, B. Li, E. T. Kiesewetter, A. H. Hoveyda Organometallics 2012, 31, 4558.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]177. “Cu-Catalyzed Enantioselective Allylic Substitution with Readily Accessible Carbonyl- and Acetal-Containing Vinylboron Reagents,” F. Gao, J. L. Carr, A. H. Hoveyda Angew. Chem., Int. Ed. 2012, 51, 6613.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]176. “A Robust, Efficient and Highly Enantioselective Method for Synthesis of Homopropargyl Amines,” E. M. Vieira, F. Haeffner, M. L. Snapper, A. H. Hoveyda Angew. Chem., Int. Ed. 2012, 51, 6618.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]175. “Metal-Free Catalytic Enantioselective C-B Bond Formation: (Pinacolato)boron Conjugate Additions to α,β-Unsaturated Ketones, Esters, Weinreb Amides, and Aldehydes Promoted by Chiral N-Heterocyclic Carbenes,” H. Wu, S. Radomkit, J. M. O’Brien, A. H. Hoveyda J. Am. Chem. Soc. 2012, 134, 8277.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]174. “Enol Ethers as Substrates for Efficient Z– and Enantioselective Ring-Opening/Cross-Metathesis Reactions Promoted by Stereogenic-at-Mo Complexes. Utility in Chemical Synthesis and Mechanistic Attributes,” M. Yu, I. Ibrahem, M. Hasegawa, R. R. Schrock, A. H. Hoveyda J. Am. Chem. Soc. 2012, 134, 2788.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]173. “Site- and Enantioselective Formation of Allene-Bearing Tertiary or Quaternary Carbon Stereogenic Centers through NHC-Cu-Catalyzed Allylic Substitution,” B. Jung, A. H. Hoveyda J. Am. Chem. Soc. 2012, 134, 1490.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]172. “Z-Selective Olefin Metathesis Reactions Promoted by Tungsten Oxo Alkylidene Complexes,” D. V. Peryshkov, R. R. Schrock, M. K. Takase, P. Müller, A. H. Hoveyda J. Am. Chem. Soc. 2011, 133, 20754.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]171. “Synthesis of Macrocyclic Natural Products by Catalyst-Controlled Stereoselective Ring-Closing Metathesis,” M. Yu, C. Wang, A. F. Kyle, P. Jakubec, D. J. Dixon, R. R. Schrock, A. H. Hoveyda Nature 2011, 479, 88.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]170. “Isolation of Pure Disubstituted E Olefins through Mo-Catalyzed Z-Selective Ethenolysis of Stereoisomeric Mixtures,” S. C. Marinescu, D. S. Levine, Y. Zhao, R. R. Schrock, A. H. Hoveyda J. Am. Chem. Soc. 2011, 133, 11512.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]169. “Regiodivergent Reactions through Catalytic Enantioselective Silylation of Chiral Diols. Synthesis of Sapinofuranone A,” J. M. Rodrigo, Y. Zhao, A. H. Hoveyda, M. L. Snapper Org. Lett. 2011, 13, 3778.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]168. “NHC-Cu-Catalyzed Enantioselective Hydroboration of Acyclic and Exocyclic 1,1-Disubstituted Aryl Alkenes,” R. Corberan, N. W. Mszar, A. H. Hoveyda Angew. Chem., Int. Ed. 2011, 50, 7079.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]167. “Metal-Free Catalytic C-Si Bond Formation in an Aqueous Medium. Enantioselective NHC-Catalyzed Silyl Conjugate Additions to Cyclic and Acyclic α,β-Unsaturated Carbonyls,” J. M. O’Brien, A. H. Hoveyda J. Am. Chem. Soc. 2011, 133, 7712.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]166. “Highly Selective Methods for Synthesis of Internal (α-) Vinylboronates through Efficient NHC-Cu-Catalyzed Hydroboration of Terminal Alkynes. Utility in Chemical Synthesis and Mechanistic Basis for Selectivity,” H. Jang, A. R. Zhugralin, Y. Lee, A. H. Hoveyda J. Am. Chem. Soc. 2011, 133, 7859.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]165. “Room-Temperature Z-Selective Homocoupling of α-Olefins by Tungsten Catalysts,” S. C. Marinescu, R. R. Schrock, P. Müller, M. K. Takase, A. H. Hoveyda Organometallics 2011, 30, 1780.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]164. “Enantioselective Synthesis of Alkyne-Substituted Quaternary Carbon Stereogenic Centers through NHC-Cu-Catalyzed Allylic Substitution Reactions with (i-Bu)2(Alkynyl)aluminum Reagents,” J. A. Dabrowski, F. Gao, A. H. Hoveyda J. Am. Chem. Soc. 2011, 133, 4778.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]163. “Catalytic Z-Selective Olefin Cross-Metathesis for Natural Product Synthesis,” S. J. Meek, R. V. O’Brien, J. Llaveria, R. R. Schrock, A. H. Hoveyda Nature 2011, 471, 461.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]162. “Enantioselective Synthesis of Homoallylic Amines through Reactions of (Pinacolato)allylborons with Aryl-, Heteroaryl-, Alkyl- or Alkene-Substituted Aldimines Catalyzed by Chiral C-Symmetric NHC-Cu-Complexes,” E. M. Vieira, M. L. Snapper, A. H. Hoveyda J. Am. Chem. Soc. 2011, 133, 3332.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]161. “Endo-Selective Enyne Ring-Closing Metathesis Promoted by Stereogenic-at-W Mono-Pyrrolide Complexes,” Y. Zhao, A. H. Hoveyda, R. R. Schrock Org. Lett. 2011, 13, 784.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” locked=”off” /][et_pb_text _builder_version=”4.0.3″]160. “Formation of Vinyl-, Vinylhalide- or Acyl-Substituted Quaternary Carbon Stereogenic Centers through NHC-Cu-Catalyzed Enantioselective Conjugate Additions of Si-Containing Vinylaluminums to β-Substituted Cyclic Enones,” T. L. May, J. A. Dabrowski, A. H. Hoveyda J. Am. Chem. Soc. 2011, 133, 736.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” locked=”off” /][et_pb_text _builder_version=”4.0.3″]159. “Synthesis of Quaternary Carbon Stereogenic Centers through Enantioselective Cu-Catalyzed Allylic Substitutions with Vinyaluminum Reagents,” F. Gao, K. P. McGrath, Y. Lee, A. H. Hoveyda J. Am. Chem. Soc. 2010, 132, 14315.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]158. “Quaternary Carbon Stereogenic Centers through Copper-Catalyzed Enantioselective Allylic Substitutions with Readily Accessible Aryl- or Hetero-aryllithium Reagents and Aluminum Chlorides,” F. Gao, Y. Lee, K. Mandai, A. H. Hoveyda Angew. Chem., Int. Ed. 2010, 49, 8370.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]157. “α -Selective Ni-Catalyzed Hydroalumination of Aryl- and Alkyl-Substituted Terminal Alkynes. Practical Syntheses of Internal Vinyl Aluminums, Halides or Boronates,” F. Gao, A. H. Hoveyda J. Am. Chem. Soc. 2010, 132, 10961.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]155. “Enantioselective Synthesis of Allylboronates Bearing a Tertiary or Quaternary B-Substituted Stereogenic Carbon by NHC-Cu-Catalyzed Substitution Reactions,” A. Guzman-Martinez, A. H. Hoveyda J. Am. Chem. Soc. 2010, 132, 10634.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]154. “Enantioselective Conjugate Silyl Additions to Cyclic and Acyclic Unsaturated Carbonyls Catalyzed by Cu Complexes of Chiral N-Heterocyclic Carbenes,” K.-S. Lee, A. H. Hoveyda J. Am. Chem. Soc. 2010, 132, 2898.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]153. “Stereoisomerically Pure Trisubstituted Vinylaluminum Reagents and their Utility in Cu-Catalyzed Enantioselective Synthesis of 1,4-Dienes Containing Z or E alkenes,” K. Akiyama, F. Gao, A. H. Hoveyda Angew. Chem., Int. Ed. 2010, 49, 419.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]152. “Vicinal Diboronates in High Enantiomeric Purity through Tandem Site-Selective NHC-Cu-Catalyzed Boron-Copper Additions to Terminal Alkynes,” Y. Lee, H. Jang, A. H. Hoveyda J. Am. Chem. Soc. 2009, 131, 18234.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]151. “Highly Z-Selective Metathesis Homocoupling of Terminal Olefins,” A. J. Jiang, Y. Zhao, R. R. Schrock, A. H. Hoveyda J. Am. Chem. Soc. 2009, 131, 16630.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]150. “The Significance of Degenerate Processes to Enantioselective Olefin Metathesis Reactions Promoted by Stereogenic-at-Mo Complexes,” S. J. Meek, S. J. Malcolmson, B. Li, R. R. Schrock, A. H. Hoveyda J. Am. Chem. Soc. 2009, 131, 16407.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]149. “Ethenolysis Reactions Catalyzed by Imido Alkylidene Monoaryloxide Monopyrrolide (MAP) Complexes of Molybdenum,” S. C. Marinescu, R. R. Schrock, P. Müller, A. H. Hoveyda J. Am. Chem. Soc. 2009, 131, 10840.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]148. “Stereogenic-at-Metal Zn- and Al-based N-Heterocyclic Carbene (NHC) Complexes as Bifunctional Catalysts in Cu-Free Enantioselective Allylic Alkylations,” Y. Lee, B. Li, A. H. Hoveyda J. Am. Chem. Soc. 2009, 131, 11625.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]147. “endo-Selective Enyne Ring-Closing Metathesis Promoted by Stereogenic-at-Mo Monoalkoxide and Monoaryloxide Complexes. Efficient Synthesis of Cyclic Dienes Not Accessible through Reactions with Ru Carbenes,” Y.-J. Lee, R. R. Schrock, A. H. Hoveyda J. Am. Chem. Soc. 2009, 131, 10652.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]146. “H-Bonding as an Control Element in Stereoselective Ru-Catalyzed Olefin Metathesis,” A. H. Hoveyda, P. J. Lombardi, R. V. O’Brien, A. R. Zhugralin J. Am. Chem. Soc. 2009, 131, 8378.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]145. “Z-Selective Olefin Metathesis Processes Catalyzed by a Molybdenum Hexaisopropylterphenoxide Monopyrrolide Complex,” M. M. Flook, A. J. Jiang, R. R. Schrock, P. Müller, A. H. Hoveyda J. Am. Chem. Soc. 2009, 131, 7962.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]144. “Monodentate Non-C2-Symmetric Chiral N-Heterocyclic Carbene Complexes for Enantioselective Synthesis. Cu-Catalyzed Conjugate Additions of Aryl- and Alkenylsilylfluorides to Cyclic Enones,” K.-S. Lee, A. H. Hoveyda J. Org. Chem. 2009, 74, 4455.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]143. “Efficient C-B Bond Formation Promoted by N-Heterocyclic Carbenes. Synthesis of Tertiary and Quaternary B-Substituted Carbons through Metal-Free Catalytic Boron Conjugate Additions to Cyclic and Acyclic α,β-Unsaturated Carbonyls,” K.-S. Lee, A. R. Zhugralin, A. H. Hoveyda J. Am. Chem. Soc. 2009, 131, 7253.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]142. “Efficient Boron-Copper Additions to Aryl-Substituted Alkenes Promoted by NHC-Based Catalysts. Enantioselective Cu-Catalyzed Hydroboration Reactions,” Y. Lee, A. H. Hoveyda J. Am. Chem. Soc. 2009, 131, 3160.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]141. “Highly Z– and Enantioselective Ring-Opening/Cross Metathesis Reactions Catalyzed by Stereogenic-at-Mo Adamantylimido Complexes,” I. Ibrahem, M. Yu, R. R. Schrock, A. H. Hoveyda J. Am. Chem. Soc. 2009, 131, 3844.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]140. “Design and Stereoselective Preparation of a New Class of Chiral Olefin Metathesis Catalysts and Application to Enantioselective Synthesis of Quebrachamine. Catalyst Development Inspired by Natural Product Synthesis,” E. S. Sattely, S. J. Meek, S. J. Malcolmson, R. R. Schrock, A. H. Hoveyda J. Am. Chem. Soc. 2009, 131, 943.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]139. “Inversion of Configuration at the Metal in Diastereomeric Imido Alkylidene Monoaryloxide Monopyrrolide (MAP) Complexes of Molybdenum,” S. C. Marinescu, R. R. Schrock, B. Li, A. H. Hoveyda J. Am. Chem. Soc. 2009, 131, 58.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]138. “Enantioselective Synthesis of P-Stereogenic Phosphinates and Phosphine Oxides by Mo-Catalyzed Asymmetric Ring-Closing Metathesis,” J. S. Harvey, S. J. Malcolmson, K. S. Dunne, S. J. Meek, A. L. Thompson, R. R. Schrock, A. H. Hoveyda, V. Gouverneur Angew. Chem., Int. Ed. 2009, 48, 762.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]137. “Catalytic Enantioselective Silylation of Acyclic and Cyclic Triols and Application to Total Syntheses of Cleroindicins D, F, and C,” Z. You, A. H. Hoveyda, M. L. Snapper Angew. Chem., Int. Ed. 2009, 48, 547.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]136. “Ag-Catalyzed Diastereo- and Enantioselective Vinylogous Mannich Reactions of α-Ketoimine Esters. Development of a Method and Investigation of its Mechanism,” L. C. Wieland, E. M. Vieira, M. L. Snapper, A. H. Hoveyda J. Am. Chem. Soc. 2009, 131, 570.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]135. “Three-Component Ag-Catalyzed Enantioselective Vinylogous Mannich and Aza-Diels-Alder Reactions with Alkyl-Substituted Aldehydes,” H. Mandai, K. Mandai, M. L. Snapper, A. H. Hoveyda J. Am. Chem. Soc. 2008, 130, 17961.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]134. “A New Class of Chiral Catalysts for Enantioselective Alkene Metathesis,” S. J. Malcolmson, S. J. Meek, E. S. Sattely, R. R, Schrock, A. H. Hoveyda Nature 2008, 456, 933.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]133. “Enantioselective Total Synthesis of Clavirolide C. Applications of Cu-Catalyzed Asymmetric Conjugate Additions and Ru-Catalyzed Ring-Closing Methathesis,” M. K. Brown, A. H. Hoveyda J. Am. Chem. Soc. 2008, 130, 12904.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]132. “Enantioselective Synthesis of All-Carbon Quaternary Stereogenic Centers by Catalytic Asymmetric Conjugate Additions of Alkyl and Aryl Aluminum Reagents to Five-, Six-, and Seven-Membered-Ring β-Substituted Cyclic Enones,” T. L. May, M. K. Brown, A. H. Hoveyda Angew. Chem., Int. Ed. 2008, 47, 7358.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]131. “Al-Catalyzed Asymmetric Alkylations of Pyridyl-Substituted Alkynyl Ketones with Dialkylzinc Reagents,” D. K. Friel, M. L. Snapper, A. H. Hoveyda J. Am. Chem. Soc. 2008, 130, 9942.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]130. “Catalytic Asymmetric Alkylations of Ketoimines. Enantioselective Synthesis of N-Substituted Quaternary Carbon Stereogenic Centers by Zr-Catalyzed Additions of Dialkylzinc Reagents to Aryl-, Alkyl- and Trifluoroalkyl-Substituted Ketoimines,” P. Fu, M. L. Snapper, A. H. Hoveyda J. Am. Chem. Soc. 2008, 130, 5530.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]129. “Highly Site- and Enantioselective Cu-Catalyzed Allylic Alkylation Reactions with Easily Accessible Vinylaluminum Reagents,” Y. Lee, K. Akiyama, D. Gillingham, M. K. Brown, A. H. Hoveyda J. Am. Chem. Soc. 2008, 130, 446.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]128. “Kinetic Resolution of 1,2-Diols through Highly Site- and Enantioselective Catalytic Silylation,” Y. Zhao, A. W. Mitra, A. H. Hoveyda, M. L. Snapper Angew. Chem., Int. Ed. 2007, 46, 8471.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]127. “Synthesis of Monoalkoxide Monopyrrolyl Complexes of the Type Mo(NR)(CHR’)(OR”)(pyrrolyl). Enyne Metathesis with High Oxidation State Catalysts,” R. Singh, R. R. Schrock, P. Müller, A. H. Hoveyda J. Am. Chem. Soc. 2007, 129, 12654.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]126. “Cu-Catalyzed Asymmetric Conjugate Additions of Dialkyl- and Diarylzinc Reagents to Acyclic β-Silyl-α , β-Unsaturated Ketones. Synthesis of Allylsilanes in High Diastereo- and Enantiomeric Purity,” M. A. Kacprzynski, S. A. Kazane, T. L. May, A. H. Hoveyda Org. Lett. 2007, 9, 3187.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]125. “Comparison of Ru- and Mo- Based Chiral Olefin Metathesis Catalysts. Complementarity in Asymmetric Ring-Opening/Cross-Metathesis Reactions of Oxa- and Azabicycles,” G. A. Cortez, C. A. Baxter, R. R. Schrock, A. H. Hoveyda Org. Lett. 2007, 9, 2871.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]124. “Molybdenum Imido Alkylidene Metathesis Catalysts That Contain Electron-Withdrawing Biphenolates or Binaphtholates,” R. Singh, C. Czekelius, R. R. Schrock, P. M. Müller, A. H. Hoveyda Organometallics 2007, 26, 2528.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″ custom_padding=”||6px|||”]122. “Efficient Enantioselective Synthesis of Piperidines through Catalytic Asymmetric Ring-Opening/Cross Metathesis Reactions,” G. A. Cortez, R. R. Schrock, A. H. Hoveyda Angew. Chem., Int. Ed. 2007, 46, 4534.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]121. “Directed Catalytic Asymmetric Olefin Metathesis. Selectivity Control by Enoate and Ynoate Groups in Ru-Catalyzed Asymmetric Ring-Opening/Cross Metathesis,” R. E. Guidici, A. H. Hoveyda J. Am. Chem. Soc. 2007, 129, 3824.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]120. “Chiral N-Heterocyclic Carbenes in Natural Product Synthesis. Application of Ru-Catalyzed Asymmetric Ring-Opening/Cross Metathesis and Cu-Catalyzed Allylic Alkylation to Total Synthesis of Baconipyrone C,” D. G. Gillingham, A. H. Hoveyda Angew. Chem., Int. Ed. 2007, 46, 3860.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]119. “New Enantiomerically Pure Alkyimido Molybdenum-Based Alkylidene Complexes. Synthesis, Characterization, and Activity as Chiral Olefin Metathesis Catalysts,” T. S. Pilyugina, R. R. Schrock, P. Müller, A. H. Hoveyda Organometallics 2007, 26, 831.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]118. “All-Carbon Quaternary Stereogenic Centers by Enantioselective Cu-Catalyzed Conjugate Additions Promoted by a Chiral N-Heterocyclic Carbene,” M. K. Brown, T. L. May, C. A. Baxter, A. H. Hoveyda Angew. Chem., Int. Ed. 2007, 46, 1097.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]117. “Dipyrrolyl Precursors to Bisalkoxide Molybdenum Olefin Metathesis Catalysts,” A. S. Hock, R. R. Schrock, A. H. Hoveyda J. Am. Chem. Soc. 2006, 128, 16373.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]116. “Lewis Base Activation of Grignard Reagents with N-Heterocyclic Carbenes. Cu-Free Catalytic Enantioselective Additions to γ-Chloro α -,β-Unsaturated Esters,” Y. Lee, A. H. Hoveyda J. Am. Chem. Soc. 2006, 128, 15604.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]115. “A Highly Efficient and Practical Method for Catalytic Asymmetric Vinylogous Mannich (AVM) Reactions,” E. L. Carswell, M. L. Snapper, A. H. Hoveyda Angew. Chem., Int. Ed. 2006, 45, 7230.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]114. “Diphenylamido Precursors to Bisalkoxide Molybdenum Olefin Metathesis Catalysts,” A. Sinha, R. R. Schrock, P. Muller, A. H. Hoveyda Organometallics 2006, 25, 4621.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]113. “Enantioselective Silyl Protection of Alcohols Catalysed by an Amino Acid-Based Small-Molecule,” Y. Zhao, J. Rodrigo, A. H. Hoveyda, M. L. Snapper Nature 2006, 443, 67.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]112. “A Practical Method for Enantioselective Synthesis of All-Carbon Quaternary Stereogenic Centers through NHC-Cu-Catalyzed Conjugate Additions of Alkyl- and Arylzinc Reagents to β-Substituted Cyclic Enones,” K.-S. Lee, M. K. Brown, A. W. Hird, A. H. Hoveyda J. Am. Chem. Soc. 2006, 128, 7182.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]111. “A Chiral Ag-based Catalyst for Practical, Efficient and Highly Enantioselective Additions of Enolsilanes to α-Ketoesters,” L. C. Akullian, M. L. Snapper, A. H. Hoveyda J. Am. Chem. Soc. 2006, 128, 6532.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]110. “Operationally Simple, Efficient, and Diastereoselective Synthesis of cis-2,6-Disubstituted-4-Methylene Tetrahydropyrans Catalyzed by Triflic Acid,” A. Puglisi, A.-L. Lee, R. R. Schrock, A. H. Hoveyda Org. Lett. 2006, 8, 1871.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]109. “Enantioselective Synthesis of Cyclic Enol Ethers and All-Carbon Quaternary Stereogenic Centers through Catalytic Asymmetric Ring-Closing Metathesis,” A.-L. Lee, S. J. Malcolmson, A. Puglisi, R. R. Schrock, A. H. Hoveyda J. Am. Chem. Soc. 2006, 128, 5153.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]108. “Al-Catalyzed Enantioselective Alkylation of α-Ketoesters by Dialkylzinc Reagents. Enhancement of Enantioselectivity and Reactivity by an Achiral Lewis Base Additive,” L. C. Wieland, H. Deng, M. L. Snapper, A. H. Hoveyda J. Am. Chem. Soc. 2005, 127, 15453.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]107. “Catalytic Enantioselective Alkylations of Tetrasubstituted Olefins. Synthesis of All-Carbon Quaternary Stereogenic Centers through Cu-Catalyzed Asymmetric Conjugate Additions of Alkylzinc Reagents to Enones,” A. W. Hird, A. H. Hoveyda J. Am. Chem. Soc. 2005, 127, 14988.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]106. “Highly Enantioselective Cu-Catalyzed Conjugate Additions of Dialkylzinc Reagents to Unsaturated Furanones and Pyranones: Preparation of Air Stable and Catalytically Active Cu.Peptide Complexes,” M. K. Brown, S. J. Degrado, A. H. Hoveyda Angew. Chem., Int. Ed. 2005, 44, 5306.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]105. “Proline-Based N-Oxides as Readily Available and Modular Chiral Catalysts. Enantioselective Reactions of Allyltrichlorosilane with Aldehydes,” J. F. Traverse, Y. Zhao, A. H. Hoveyda, M. L. Snapper Org. Lett. 2005, 7, 3151.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]104. “Practical and Highly Enantioselective Synthesis of β-Alkynyl-β-amino Esters through Ag-Catalyzed Asymmetric Mannich Reactions of Silylketene Acetals and Alkynyl Imines,” N. S. Josephsohn, E. L. Carswell, M. L. Snapper, A. H. Hoveyda Org. Lett. 2005, 7, 2711.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]103. “Enantioselective Synthesis of Cyclic Amides and Amines through Mo-Catalyzed Asymmetric Ring-Closing Metathesis,” E. S. Sattely, G. A. Cortez, D. C. Moebius, R. R. Schrock, A. H. Hoveyda J. Am. Chem. Soc. 2005, 127, 8526.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]102. “Isocomplestatin: Total Synthesis and Stereochemical Revision,” T. Shinohara, H. Deng, M. L. Snapper, A. H. Hoveyda J. Am. Chem. Soc. 2005, 127, 7334.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]101. “A Readily Available Chiral Ag-Based N-Heterocyclic Carbene Complex for Use in Efficient and Highly Enantioselective Ru-Catalyzed Olefin Metathesis and Cu-Catalyzed Allylic Alkylation Reactions,” J. J. Van Veldhuizen, J. E. Campbell, R. E. Guidici, A. H. Hoveyda J. Am. Chem. Soc. 2005, 127, 6877.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]100. “Enantioselective Synthesis of Nitroalkanes Bearing All-Carbon Quaternary Stereogenic Centers through Cu-Catalyzed Asymmetric Conjugate Additions,” J. Wu, D. M. Mampreian, A. H. Hoveyda J. Am. Chem. Soc. 2005, 127, 4584.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]99. “Catalytic Enantioselective Synthesis of Quaternary All-Carbon Stereogenic Centers. Preparation of α,α’-Disubstituted-β,γ-Unsaturated Esters through Cu-Catalyzed Asymmetric Allylic Alkylations,” K. E. Murphy, A. H. Hoveyda Org Lett. 2005, 7, 1255.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]98. “Asymmetric Synthesis of Acyclic Amines Through Zr- and Hf-Catalyzed Enantioselective Addition of Alkylzinc Reagents to Imines,” L. C. Akullian, J. R. Porter, J. F. Traverse, M. L. Snapper, A. H. Hoveyda Adv. Synth. Catal. 2005, 347, 417.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]97. “Regarding the Mechanism of Olefin Metathesis with Sol-Gel-Supported Ru-Based Complexes Bearing a Bidentate Carbene Ligand. Spectroscopic Evidence for Return of the Propagating Ru Carbene,” J. S. Kingsbury, A. H. Hoveyda J. Am. Chem. Soc. 2005, 127, 4510.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]96. “Efficient Enantioselective Synthesis of Functionalized Tetrahydropyrans by Ru-Catalyzed Asymmetric Ring-Opening Metathesis/Cross Metathesis (AROM/CM),” D. G. Gillingham, O. Kataoka, S. B. Garber, A. H. Hoveyda J. Am. Chem. Soc. 2004, 126, 12288.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]95. “Bidentate NHC-Based Chiral Ligands for Efficient Cu-Catalyzed Enantioselective Allylic Alkylations: Structure and Activity of an Air-Stable Chiral Cu Complex,” A. O. Larsen, W. Leu, C. N. Oberhuber, J. E. Campbell, A. H. Hoveyda J. Am. Chem. Soc. 2004, 126, 11130.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]94. “Efficient Cu-Catalyzed Asymmetric Conjugate Additions of Alkylzinc Reagents to Aromatic and Aliphatic Acyclic Nitroalkenes,” D. M. Mampreian, A. H. Hoveyda Org. Lett., 2004, 6, 2829.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]93. “Investigations of Reactions between Chiral Molybdenum Imido Alkylidene Complexes and Ethylene: Observation of Unsolvated Base-Free Methylene Complexes, Metalacyclobutane and Metalacyclopentane Complexes, and Molybdenum(IV) Olefin Complexes,” W. C. P. Tsang, J. Y. Jamieson, S. L. Aeilts, K. C. Hultzsch, R. R. Schrock, A. H. Hoveyda Organometallics, 2004, 23, 1997.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]92. “Supported Chiral Mo-Based Complexes as Efficient Catalysts for Enantioselective Olefin Metathesis,” S. J. Dolman, K. C. Hultzsch, F. Pezet, X. Teng, A. H. Hoveyda, R. R. Schrock J. Am. Chem. Soc., 2004, 126, 10945.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]91. “Enantioselective Synthesis of Cyclic Allylboronates by Mo-catalyzed Asymmetric Ring-Closing Metathesis (ARCM). A One-Pot Protocol for Net Catalytic Enantioselective Cross Metathesis,” J. A. Jernelius, R. R. Schrock, A. H. Hoveyda Tetrahedron, 2004, 60, 7345.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]90. “Cu-Catalyzed Asymmetric Allylic Alkylations of Aromatic and Aliphatic Phosphates with Alkylzinc Reagents. An Effective Method for Enantioselective Synthesis of Tertiary and Quaternary Carbons, ” M. A. Kacprzynski, A. H. Hoveyda J. Am. Chem. Soc. 2004, 126, 10676.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]89. “Ag-Catalyzed Asymmetric Mannich Reactions of Enol Ethers with Aryl, Alkyl, Alkenyl, and Alkynyl Imines,” N. S. Josephsohn, M. L. Snapper, A. H. Hoveyda J. Am. Chem. Soc. 2004, 126, 3734.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]88. “Catalytic Homologation of Vinyltributylstannane to Allyltributylstannae by Mo(IV) Complexes in the Presence of Ethylene,” R. R. Schrock, M. Duval-Lungulescu, W. C. P. Tsang, A. H. Hoveyda J. Am. Chem. Soc. 2004, 126, 1948.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]87. “Mo-Catalyzed Asymmetric Olefin Metathesis in Target-Oriented Synthesis. Enantioselective Synthesis of (+)-Africanol,” G. S. Weatherhead, G. A. Cortez, R. R. Schrock, A. H. Hoveyda Proc. Nat. Acad. Sci. 2004, 101, 5805.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]86. “Enantioselective Total Synthesis of Erogorgiaene: Applications of Asymmetric Cu-Catalyzed Conjugate Additions of Alkylzincs to Acyclic Enones,” R. R. Cesati, J. de Armas, A. H. Hoveyda J. Am. Chem. Soc. 2004, 126, 96.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]85. “Enantioselective Synthesis of Cyclic Secondary Amines through Mo-Catalyzed Asymmetric Ring-Closing Metathesis (ARCM),” S. J. Dolman, R. R. Schrock, A. H. Hoveyda Org. Lett. 2003, 5, 4899.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]84. “Chiral Ru-Based Complexes for Asymmetric Olefin Metathesis: Enhancement of Catalytic Activity through Steric and Electronic Modifications”, J. J. Van Veldhuizen, D. G. Gillingham, S. B. Garber, O. Kataoka, A. H. Hoveyda J. Am. Chem. Soc. 2003, 125, 12502.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]83. “Three-Component Enantioselective Synthesis of Propargylamines through Zr-Catalyzed Additions of Alkyl Zinc Reagents to Alkynylimines,” L. C. Akullian, M. L. Snapper, A. H. Hoveyda Angew. Chem., Int. Ed. 2003, 42, 4244.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]82. “Enantioselective Synthesis of Propargylamines through Zr-Catalyzed Addition of Mixed Alkynylzinc Reagents to Arylimines,” J. F. Traverse, A. H. Hoveyda, M. L. Snapper Org. Lett. 2003, 5, 3273.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]81. “Total Synthesis of Anti-HIV Chloropeptin I,” H. Deng, J-K. Jung, T. Liu, K. W. Kuntz, M. L. Snapper, A. H. Hoveyda J. Am. Chem. Soc. 2003, 125, 9032.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]80. “Enantioselective Synthesis of α-Alkyl-β,γ-unsaturated Esters through Efficient Cu-Catalyzed Allylic Alkylations,” K. E. Murphy, A. H. Hoveyda J. Am. Chem. Soc. 2003, 125, 4690.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]79. “Efficient and Practical Ag-Catalyzed Cycloadditions between Arylimines and the Danishefsky Diene,” N. S. Josephsohn, M. L. Snapper, A. H. Hoveyda J. Am. Chem. Soc. 2003, 125, 4018.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]78. “Cu-Catalyzed Enantioselective Conjugate Additions of Alkyl Zinc Reagents to Unsaturated N-Acyloxazolidinones Promoted by a Chiral Triamide Phosphane,” A. W. Hird, A. H. Hoveyda Angew. Chem., Int. Ed. 2003, 42, 1276.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]77. “An Enantiomerically Pure Adamantylimido Molybdenym Alkylidene Complex. An Effective New Catalyst for Enantioselective Olefin Metathesis,” W. C. P. Tsang, J. A. Jernelius, G. A. Cortez, G. S. Weatherhead, R. R. Schrock, A. H. Hoveyda J. Am. Chem. Soc. 2003, 125, 2591.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]76. “Alkylidene and Metalacyclic Complexes of Tungsten that Contain a Chiral Biphenoxide Ligand. Synthesis, Asymmetric Ring-Closing Metathesis, and Mechanistic Investigations,” W. C. P. Tsang, K. C. Hultzsch, J. B. Alexander, P. J. Bonitatebus, Jr., R. R. Schrock, A. H. Hoveyda J. Am. Chem. Soc. 2003, 125, 2652.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]75. “Zr-Catalyzed Diastereo- and Enantioselective Diene Cyclizations. An Unexpected Synthesis of Chiral Aldehydes,” S. J. Degrado, J. A. Adams, A. H. Hoveyda Inorg. Chim. Acta 2003, 345, 261.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]74. “Efficient Cu-Catalyzed Asymmetric Conjugate Additions of Allylzincs to Trisubstituted Cyclic Enones,” S. J. Degrado, H. Mizutani, A. H. Hoveyda J. Am. Chem. Soc. 2002, 124, 13362.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]73. “Enhancement of Enantioselectivity by THF in Asymmetric Mo-Catalyzed Olefin Metathesis. Catalytic Enantioselective Synthesis of Cyclic Tertiary Ethers and Spirocycles,” X. Teng, D. R. Cefalo, R. R. Schrock, A. H. Hoveyda J. Am. Chem. Soc. 2002, 124, 10779.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]72. “Cu–Catalyzed Enantioselective Conjugate Addition of Alkylzincs to Cyclic Nitroalkenes: Catalytic Asymmetric Synthesis of Cyclic α-Substituted Ketones,” C. A. Luchaco-Cullis, A. H. Hoveyda J. Am. Chem. Soc. 2002, 124, 8192.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]71. “Efficient Catalytic Enantioselective Synthesis of Unsaturated Amines: Preparation of Small- and Medium-Ring Cyclic Amines through Mo-Catalyzed Asymmetric Ring-Closing Metathesis in the Absence of Solvent,” S. J. Dolman, E. S. Sattely, A. H. Hoveyda, R. R. Schrock J. Am. Chem. Soc. 2002, 124, 6991.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]70. “A Recyclable Chiral Ru Catalyst for Enantioselective Olefin Metathesis. Efficient Catalytic Asymmetric Ring-Opening/Cross Metathesis in Air,” J. J. Van Veldhuizen, S. B. Garber, J. S. Kingsbury, A. H. Hoveyda J. Am. Chem. Soc. 2002, 124, 4954.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]69. “Enantioselective Synthesis of Medium Ring Heterocycles, Tertiary Ethers and Tertiary Alcohols by Mo-Catalyzed Ring-Closing Metathesis,” A. F. Kiely, J. A. Jernelius, R. R. Schrock, A. H. Hoveyda J. Am. Chem. Soc. 2002, 124, 2868.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]68. “Olefins Turned Alkylating Agents: Diastereoselective Intramolecular Zr-Catalyzed Olefin Alkylations,” R. R. Cesati III, J. de Armas, A. H. Hoveyda Org. Lett. 2002, 4, 395.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]67. “Aluminum-Catalyzed Asymmetric Addition of TMSCN to Aromatic and Aliphatic Ketones Promoted by an Easily Accessible and Recyclable Peptide Ligand,” H. Deng, M. P. Isler, M. L. Snapper, A. H. Hoveyda Angew. Chem., Int. Ed. 2002, 41, 1009.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]66. “The First Polymer-Supported and Recyclable Chiral Catalyst for Enantioselective Olefin Metathesis,” K. C. Hultszch, J. A. Jernelius, A. H. Hoveyda, R. R. Schrock Angew. Chem., Int. Ed. 2002, 41, 589.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]65. “Cu-Catalyzed Asymmetric Conjugate Additions of Alkylzinc Reagents to Acyclic Aliphatic Enones,” H. Mizutani, S. J. Degrado, A. H. Hoveyda J. Am. Chem. Soc. 2002, 124, 779.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]64. “New Chiral Molybdenum Catalysts for Asymmetric Olefin Metathesis that Contain 3,3′-Disubstituted Octahydrobinaphtholate or 2,6-Dichlorophenylimido Ligands,” R. R. Schrock, J. Y. Jamieson, S. J. Dolman, S. A. Miller, P. J. Bonitatebus, A. H. Hoveyda Organometallics 2002, 21, 409.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]63. “Evaluation of Enantiomerically Pure Binaphthol-Based Molybdenum Catalysts for Asymmetric Olefin Metathesis Reactions that Contain 3,3′-Diphenyl- or 3,3′-Dimesityl-Substituted Binaphtholate Ligands. Generation and Decomposition of Unsubstituted Molybdacyclobutane Complexes,” W. C. P. Tsang, R. R. Schrock, A. H. Hoveyda Organometallics 2001, 20, 5658.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]62. “Immobilization of Olefin Metathesis Catalysts on Monolithic Sol-Gel. Practical, Efficient and Easily Recyclable Catalysts for Organic and Combinatorial Synthesis,” J. S. Kingsbury, S. B. Garber, J. M. Giftos, B. L. Gray, M. M. Okamoto, R. A. Farrer, J. T. Fourkas, A. H. Hoveyda Angew. Chem., Int. Ed. 2001, 40, 4251.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]61. “Mechanism of Enantioselective Ti-Catalyzed Strecker Reaction: Peptide-Based Metal Complexes as Bifunctional Catalysts,” N. S. Josephson, K. W. Kuntz, M. L. Snapper, A. H. Hoveyda J. Am. Chem. Soc. 2001, 123, 11594.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]60. “Three-Component Catalytic Asymmetric Synthesis of Aliphatic Amines,” J. R. Porter, J. F. Traverse, A. H. Hoveyda, M. L. Snapper J. Am. Chem. Soc. 2001, 123, 10409.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]59. “Molybdenum Imido Alkylidene Complexes Containing Biphen Ligands That Have Silyl Groups Attached through the 6 and 6′ Methyl Group Carbon Atoms,” K. C. Hultszch, P. J. Bonitatebus, J. Jernelius, R. R. Schrock, A. H. Hoveyda Organometallics 2001, 20, 4705.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]58. “Zr-Catalyzed Electrophilic Carbomagnesation of Aryl Olefins. Mechanism-Based Control of Zr-Mg Ligand Exchange,” J. de Armas, A. H. Hoveyda Org. Lett. 2001, 3, 2097.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]57. “Catalytic Asymmetric Ring-Opening Metathesis/Cross Metathesis (AROM/CM) Reactions. Mechanism and Application to Enantioselective Synthesis of Functionalized Cyclopentanes,” D. S. La, E. S. Sattely, J. G. Ford, R. R. Schrock, A. H. Hoveyda J. Am.Chem. Soc. 2001, 123, 7767.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]56. “Modular Pyridinyl Peptide Ligands in Asymmetric Catalysis: Enantioselective Synthesis of Quaternary Carbon Atoms Through Cu-Catalyzed Allylic Substitutions,” C. A. Luchaco-Cullis, H. Mizutani, K. E. Murphy, A. H. Hoveyda Angew. Chem., Int. Ed. 2001, 40, 1456.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]55. “A Readily Available and User-Friendly Chiral Catalyst for Efficient Enantioselective Olefin Metathesis,” S. L. Aeilts, D. R. Cefalo, P. J. Bonitatebus, Jr., J. H. Houser, A. H. Hoveyda, R. R. Schrock Angew. Chem., Int. Ed. 2001, 40, 1452.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]54. “Enantioselective Synthesis of Unsaturated Cyclic Tertiary Ethers by Mo-Catalyzed Olefin Metathesis,” D. R. Cefalo, A. F. Kiely, M. Wuchrer. J. Y. Jamieson, R. R. Schrock, A. H. Hoveyda J. Am. Chem. Soc. 2001, 123, 3139.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]53. “Cross-Metathesis Reaction. Generation of Highly Functionalized Olefins from Unsaturated Alcohols,” J. Cossy, S. BouzBouz, A. H. Hoveyda J. Organomet. Chem. 2001, 634, 216.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]52. “Enantioselective Synthesis of Arylamines Through Zr-Catalyzed Addition of Dialkylzincs to Imines. Reaction Development by Screening of Parallel Libraries,” J. R. Porter, J. F. Traverse, A. H. Hoveyda, M. L. Snapper J. Am. Chem. Soc. 2001, 123, 984.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]51. “Modular Peptide-Based Phosphine Ligands in Asymmetric Catalysis: Efficient and Enantioselective Cu-Catalyzed Conjugate Additions to Five-, and Six- and Seven-Membered Cyclic Enones,” S. J. Degrado, H. Mizutani, A. H. Hoveyda J. Am. Chem. Soc. 2001, 123, 755.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]50. “Synthesis of Molybdenum Imido Alkylidene Complexes that Contain 3,3′-Dialkyl-5,5′,6,6′-tetramethyl-1,1′-biphenyl-2,2′-diolates (Alkyl = t-Bu or Adamantyl). Catalysts for Enantioselective Olefin Metathesis Reactions,” J. B. Alexander, R. R. Schrock, W. M. Davis, W., K. C. Hultzsh, A. H. Hoveyda, J. H. Houser, Organometallics 2000, 19, 3700.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]49. “Modular Mo-Based Catalysts for Efficient Asymmetric Olefin Metathesis. Catalytic Enantioselective Synthesis of Cyclic Ethers and Acetals,” G. S. Weatherhead, J. H. Houser, J. G. Ford, J. Y. Jamieson, R. R. Schrock, A. H. Hoveyda Tetrahedron Lett. 2000, 41, 9553. (Special issue in celebration of the 80th birthday of Professor Harry H. Wasserman)
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]48. “Efficient and Recyclable Monomeric and Dendritic Ru-Based Metathesis Catalysts,” S. B. Garber, J. S. Kingsbury, B. L. Gray, A. H. Hoveyda J. Am. Chem. Soc. 2000, 122, 8168.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]47. “Zr-Catalyzed Olefin Alkylations and Allylic Substitution Reactions with Electrophiles,” J. de Armas, S. P. Kolis, A. Hoveyda J. Am. Chem. Soc. 2000, 122, 5977.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]46.“Ti-Catalyzed Regio- and Enantioselective Synthesis of Unsaturated α-Amino Nitriles, Amides and Acids. Catalyst Identification through Screening of Parallel Libraries,” J. R. Porter, W. G. Wirschun, K. W. Kuntz, M. L. Snapper, A. H. Hoveyda J. Am. Chem. Soc. 2000, 122, 2657.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]45. “Synthesis of Molybdenum Imido Alkylidene Complexes Containing N,N’-Disubstituted 2,2′-Bisamido-1,1′-binaphthyl Ligands,” J. Y. Jamieson, R. R. Schrock, W. M. Davis, P. J. Bonitatebus, S. S. Zhu, A. H. Hoveyda Organometallics 2000, 19, 925.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]44. “Tandem Catalytic Asymmetric Ring-Opening Metathesis/Ring-Closing Metathesis,” G. S. Weatherhead, G. J. Ford, E. J. Alexanian, R. R. Schrock, A. H. Hoveyda J. Am. Chem. Soc. 2000, 122, 1828.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]43. “Zr-Catalyzed Kinetic Resolution of Aliphatic Cyclic Allylic Ethers. Carbocycles to Heterocycles by Ru- and Mo-Catalyzed Ring-Opening and Ring-Closing Metathesis,” J. A. Adams, J. G. Ford, P. J. Stamatos, A. H. Hoveyda J. Org. Chem 1999, 64, 9690.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]42. “Tandem Catalytic Asymmetric Ring-Opening Metathesis/Ring-Closing Metathesis,” D. S. La, J. G. Ford, E. S. Sattely, P. J. Bonitatebus, R. R. Schrock, A. H. Hoveyda J. Am. Chem. Soc. 1999, 121, 11603.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]41. “Chiral Mo-Binol Complexes: Activity, Synthesis, and Structure. Efficient Enantioselective Six-Membered Ring Synthesis through Catalytic Metathesis,” S. S. Zhu, D. R. Cefalo, D. S. La, J. Y. Jamieson, W. M. Davis, A. H. Hoveyda, R. R. Schrock J. Am. Chem. Soc. 1999, 121, 8251.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]40. “Ti-Catalyzed Enantioselective Addition of Cyanide to Imines. A Practical Synthesis of Optically Pure α-Amino Acids, ” C. A. Krueger, K. W. Kuntz, C. D. Dzierba, W. G. Wirschun, J. D. Gleason, M. L. Snapper, A. H. Hoveyda J. Am. Chem. Soc. 1999, 121, 4284.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]39. “Stereoselective Chelate-Controlled Addition of Grignard Reagents to Unsaturated Medium-Ring Heterocycles,” J. A. Adams, N. M. Heron, A. M. Koss, A. H. Hoveyda J. Org. Chem. 1999, 64, 854.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]38. “Diastereoselective Intramolecular Cycloaddition of Vinylsilanes and Silyl Nitronates. Effective Control of Remote Acyclic Asymmetry,” D. G. J. Young, E. Gomez-Bengoa, A. H. Hoveyda J. Org. Chem. 1999, 64, 692.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]37. “A Recyclable Ru-Based Metathesis Catalyst,” J. S. Kingsbury, J. P. A. Harrity, P. J. Bonitatebus, A. H. Hoveyda J. Am. Chem. Soc. 1999, 121, 791.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]36. “Mo-Catalyzed Asymmetric Synthesis of Dihydrofurans. Catalytic Kinetic Resolution and Enantioselective Desymmetrization through Ring-Closing Metathesis,” D. S. La, J. B. Alexander, D. R. Cefalo, D. D. Graf, A. H. Hoveyda, R. R. Schrock J. Am. Chem. Soc. 1998, 120, 9720.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]35. “Zr-Catalyzed Kinetic Resolution of Allylic Ethers and Mo-Catalyzed Chromene Formation in Synthesis. Enantioselective Total Synthesis of the Antihypertensive Agent (S,R,R,R)-Nebivolol,” C. W. Johannes, M. S. Visser, G. S. Weatherhead, A. H. Hoveyda J. Am. Chem. Soc. 1998, 120, 8340.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]34. “Catalytic Enantioselective Ring-Closing Metathesis by a Chiral Biphen-Mo Complex,” J. B. Alexander, D. S. La, D. R. Cefalo, A. H. Hoveyda, R. R. Schrock J. Am. Chem. Soc. 1998, 120, 4041.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]33. “Ni-Catalyzed Asymmetric Addition of Grignard Reagents to Unsaturated Cyclic Acetals. The Influence of Added Phosphine on Enantioselectivity,” E. Gomez-Bengoa, N. M. Heron, M. T. Didiuk, C. A. Luchaco, A. H. Hoveyda J. Am. Chem. Soc. 1998, 120, 7649.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]32. “Chromenes through Metal-Catalyzed Reactions of Styrenyl Ethers. Mechanism and Utility in Synthesis,” J. P. A. Harrity, D. S. La, D. R. Cefalo, M. S. Visser, A. H. Hoveyda J. Am. Chem. Soc. 1998, 120, 2343.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]31. “Phosphine-Directed Stereo- & Regioselective Ni-Catalyzed Reactions of Grignard Reagents with Allylic Ethers,” M. T. Didiuk, J. P. Morken, A. H. Hoveyda Tetrahedron 1998, 54, 1117.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]30. “Applications of Zr-Catalyzed Carbomagnesation and Mo-Catalyzed Macrocyclic Ring Closing Metathesis in Asymmetric Synthesis. Enantioselective Total Synthesis of Sch 38516 (Fluvirucin B1),” Z. Xu, C. W. Johannes, A. F. Houri, D. S. La, D. A. Cogan, G. E. Hofilena, A. H. Hoveyda J. Am. Chem. Soc. 1997, 119, 10302.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]29. “Stereoselective Heteroatom-Assisted Allylic Alkylation of Cyclic Ethers With Grignard Reagents. A Convenient Route to Enantiomerically Pure Carbocycles,” N. M. Heron, J. A. Adams, A. H. Hoveyda J. Am. Chem. Soc. 1997, 119, 6205.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]28. “Search for Chiral Catalysts Through Ligand Diversity: Substrate-Specific Catalysts and Ligand Screening on Solid Support,” K. D. Shimizu, B. M. Cole, C. A. Krueger, K. W. Kuntz, M. L. Snapper, A. H. Hoveyda Angew. Chem., Int. Ed. Engl. 1997, 36, 1704.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]27. “Synthesis of Amino Sugars Through a Highly Diastereoselective Dipolar Cycloaddition. Enantioselective Synthesis of the Carbohydrate Segment of Sch 38516,” Z. Xu, C. W. Johannes, D. S. La, G. E. Hofilena, A. H. Hoveyda Tetrahedron 1997, 53, 16377.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]26. “Ru-Catalyzed Rearrangement of Styrenyl Ethers. Enantioselective Synthesis of Chromenes Through Zr- and Ru-Catalyzed Processes,” J. P. A. Harrity, M. S. Visser, J. D. Gleason, A. H. Hoveyda J. Am. Chem. Soc. 1997, 119, 1488.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]25. “Enantioselective Total Synthesis of Antifungal Agent Sch 38516,” Z. Xu, C. W. Johannes, S. S. Salman, A. H. Hoveyda J. Am. Chem. Soc. 1996, 118, 10926.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]24. “Discovery of Chiral Catalysts through Ligand Diversity: Ti-Catalyzed Enantioselective Addition of TMSCN to meso Epoxides,” B. M. Cole, K. D. Shimizu, C. A. Kruger, J. P. A. Harrity, M. L. Snapper, A. H. Hoveyda Angew. Chem., Int. Ed. Engl. 1996, 35, 1668.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]23. “Directed Regioselective Ni-Catalyzed Alkylation and Hydride Addition of Allylic Ethers. A Remarkable Turnover in Regioselectivity,” J. P. Morken, M. T. Didiuk, A. H. Hoveyda Tetrahedron Lett. 1996, 37, 3613.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]22. “Zirconium-Catalyzed Kinetic Resolution of Cyclic Allylic Ethers. An Enantioselective Route to Unsaturated Medium Ring Systems,” M. S. Visser, J. P. A. Harrity, A. H. Hoveyda J. Am. Chem. Soc. 1996, 118, 3779.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]21. “Catalytic and Enantioselective Route to Medium-Ring Heterocycles. Asymmetric Zirconium-Catalyzed Ethylmagnesation of Seven- and Eight-Membered Rings,” M. S. Visser, N. M. Heron, M. T. Didiuk, J. F. Sagal, A. H. Hoveyda J. Am. Chem. Soc. 1996, 118, 4291.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]20. “Highly Diastereoselective Hydrosilation Reactions. Spirocyclic Siloxanes: Sources of Si-Based Lewis Acids,” D. G. J. Young, M. R. Hale, A. H. Hoveyda Tetrahedron Lett. 1996, 37, 827.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]19. “Directed Regio- and Stereoselective Nickel-Catalyzed Addition of Alkyl Grignard Reagents to Allylic Ethers,” M. T. Didiuk, J. P. Morken, A. H. Hoveyda J. Am. Chem. Soc. 1995, 117, 7273.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]18. “Cascade Catalysis in Synthesis. An Enantioselective Route to Sch 38516 (and Fluvirucin B1) Aglycon Macrolactam,” A. F. Houri, Z. Xu, D. A. Cogan, A. H. Hoveyda J. Am. Chem. Soc. 1995, 117, 2943.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]17. “Enantio-, Diastereo-, and Regioselective Zirconium-Catalyzed Carbomagnesation of Cyclic Ethers with Higher Alkyls of Magnesium. Utility in Synthesis and Mechanistic Implications,” M. T. Didiuk, C. W. Johannes, J. P. Morken, A. H. Hoveyda J. Am. Chem. Soc. 1995, 117, 7097.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]16. “Zirconocene-Catalyzed Kinetic Resolution of Dihydrofurans,” M. S. Visser, A. H. Hoveyda Tetrahedron 1995, 51, 4383.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]15. “Diastereoselective Heteroatom-Directed Conjugate Addition of Silylcuprate Reagents to Unsaturated Carbonyls. A Stereoselective Route to β-Carbonyl Siloxanes,” M. R. Hale, A. H. Hoveyda J. Org. Chem. 1994, 59, 4370.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]14. “Zirconium-Catalyzed Kinetic Resolution of Pyrans,” J. P. Morken, M. T. Didiuk, M. S. Visser, A. H. Hoveyda J. Am. Chem. Soc. 1994, 116, 3123.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]13. “Zirconium-Catalyzed Asymmetric Carbomagnesation,” J. P. Morken, M. T. Didiuk, A. H. Hoveyda J. Am. Chem. Soc. 1993, 115, 6997.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]12. “Regio- and Stereoselective Carbon-Carbon Bond Formation through Transition Metal Catalysis. The Influence of Catalyst Chirality on Selective Ethylmagnesation of Chiral, Nonracemic Alcohols and Ethers,” A. H. Hoveyda, J. P. Morken J. Org. Chem. 1993, 58, 4237.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]11. “Zirconium-Catalyzed Ethylmagnesation of Hydroxylated Terminal Alkenes; A Catalytic and Diastereoselective Carbon-Carbon Bond-Forming Reaction,” A. F. Houri, M. T. Didiuk, Z. Xu, N. R. Horan, A. H. Hoveyda J. Am. Chem. Soc. 1993, 115, 6614.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]10. “On the Mechanism of the Zirconium-Catalyzed Carbomagnesation Reaction. Efficient and Selective Catalytic Carbomagnesation with Higher Alkyls of Magnesium,” A. H. Hoveyda, J. P. Morken, A. F. Houri, Z. Xu J. Am. Chem. Soc. 1992, 114, 6692.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]9. “Rhodium (I)- and Iridium (I)-Catalyzed Hydroboration Reactions: Scope and Synthetic Applications,” D. A. Evans, G. C. Fu, A. H. Hoveyda J. Am. Chem. Soc. 1992, 114, 6671.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]8. “Siloxanes: Versatile Templates for Acyclic Stereocontrol. Synthesis of the C27-C33 Segment of Rapamycin,” M. R. Hale, A. H. Hoveyda J. Org. Chem. 1992, 57, 1643.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]7. “Stereoselective Zirconium-Catalyzed Ethylmagnesation of Homoallylic Alcohols and Ethers. The Influence of Internal Lewis Bases on Substrate Reactivity,” A. H. Hoveyda, Z. Xu, J. P. Morken, A. F. Houri J. Am. Chem. Soc. 1991, 113, 8950.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]6. “Stereoselective Formation of Carbon-Carbon Bonds Through Metal Catalysis. The Zirconium-Catalyzed Ethylmagnesation Reaction,” A. H. Hoveyda, Z. Xu J. Am. Chem. Soc. 1991, 113, 5079.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]5. “Samarium-Catalyzed Intramolecular Tishchenko Reduction of β-Hydroxy Ketones. A Stereoselective Approach to the Synthesis of Differentiated Anti 1,3-Diol Monoesters,” D. A. Evans, A. H. Hoveyda J. Am. Chem. Soc. 1990, 112, 6447.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]4. “Reduction of β-Hydroxy Ketones with Catecholborane. A Stereoselective Approach to the Synthesis of Syn-1,3-Diols,” D. A. Evans, A. H. Hoveyda J. Org. Chem. 1990, 55, 5190.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]3. “The Rhodium(I)-Catalyzed Hydroboration of Olefins. The Documentation of Regio- and Stereochemical Control in Cyclic and Acyclic Systems,” D. A. Evans, G. C. Fu, A. H. Hoveyda J. Am. Chem. Soc. 1988, 110, 6917.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]2. “Synthetic Studies of the Furan-Carbonyl Photocycloaddition Reaction. A Total Synthesis of (±)-Avenaciolide,” S. L. Schreiber, A. H. Hoveyda J. Am. Chem. Soc. 1984, 106, 7200.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]1. “A Photochemical Route to the Formation of Threo Aldols,” S. L. Schreiber, A. H. Hoveyda, H-J. Wu J. Am. Chem. Soc. 1983, 105, 660.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”25px||1px||false|false” /][/et_pb_column][/et_pb_row][/et_pb_section] [et_pb_section bb_built=”1″ module_id=”reviews” _builder_version=”4.0.3″ custom_margin=”-100px||||false|false” prev_background_color=”#000000″ next_background_color=”#000000″][et_pb_row _builder_version=”4.0.3″][et_pb_column type=”4_4″ _builder_version=”4.0.3″][et_pb_text _builder_version=”4.0.3″ header_3_text_color=”#e02b20″ custom_padding=”||0px|||”]REVIEWS, PERSPECTIVES, CONCEPT ARTICLES
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.6.0″ link_option_url=”https://onlinelibrary.wiley.com/doi/10.1002/anie.202010205″] 41. “Impact of Ethylene on Efficiency and Stereocontrol in Olefin Metathesis: When to Add It, When to Remove It,and When to Avoid It,” A. H. Hoveyda, Z. Liu, C. Qin, T. Koengeter, and Y. Mu Angew. Chem., Int. Ed. 2020, 59, 22324. [/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.6.0″ link_option_url=”https://onlinelibrary.wiley.com/doi/full/10.1002/anie.202003755″] 40. “Sulfonate N-Heterocyclic Carbene–Copper Complexes: Uniquely Effective Catalysts for Enantioselective C–C, C–B, C–H, and C–Si Bond Formation,” A. H. Hoveyda, Y. Zhou, Y. Shi, K. Brown, H. Wu, and S. Torker Angew. Chem., Int. Ed. 2020, 59, 21304. [/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.11″] 39. “Catalytic, Enantioselective, Copper–Boryl Additions to Alkenes,” A. H. Hoveyda, M. J. Koh, K. Lee, J. Lee, in Organic Syntheses, S. E. Denmark, D. Hall, Eds; 2020, Vol 100, 959. [/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.11″]38. “Different Strategies for Designing Dual-Catalytic Enantioselective Processes: From Fully Cooperative to Non-cooperative Systems,” F. Romiti, J. del Pozo, P. H. S. Paioti, S. A. Gonsales, X. Li, F. W. W. Hartrampf, A. H. Hoveyda J. Am. Chem. Soc. 2019, 141, 17952.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]37. “Organoaluminum Compounds in Catalytic Enantioselective C–C Bond Forming Reactions,” K. P. McGrath, A. H. Hoveyda in The Chemistry of Organoaluminum Compounds., Z. Rappoport, I. Marek, Eds.; Wiley, Hoboken, 2017.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]36. “Activation of B–B and B–Si Bonds and Synthesis of Organoboron and Organosilicon Compounds through Lewis Base Catalyzed Transformations,” A. Hoveyda, H. Wu, S. Radomkit, J. M. Garcia, F. Haeffner, K-S. Lee in Lewis Base Catalysis; E. Vedejs, S. E. Denmark. Eds.; VCH-Wiley, Weinheim, 2016, Vol 3, 967.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]35. “Catalyst-Controlled Stereoselective Olefin Metathesis,” A. H. Hoveyda, R. K. M. Khan, S. Torker, S. J. Malcolmson, Handbook of Metathesis (Second Edition), R. H. Grubbs, D. J. O’Leary, Eds.; VCH-Wiley, Weinheim, 2015, Vol 2, 503.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]34. “Evolution of Catalytic Stereoselective Olefin Metathesis: From Ancillary Transformation to Purveyor of Stereochemical Identity,” A. H. Hoveyda J. Org. Chem. 2014, 79, 4763.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]33. “Dichloro[[2-(1-methylethoxy-O)phenyl]- methylene](tricyclohexylphosphine) Ruthenium,” S. B. Garber, A. H. Hoveyda, R. K. M. Khan, T. J. Mann, e-EROS Encyclopedia of Reagents for Organic Synthesis
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]32. “Catalytic Enantioselective Olefin Metathesis and Natural Product Synthesis. Chiral Metal-Based Complexes that Deliver High Enantioselectivity and More,” A. H. Hoveyda, S. J. Malcolmson, S. J. Meek, A. R. Zhugralin Angew. Chem., Int. Ed. 2010, 49, 34.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]31. “Catalytic Enantioselective Olefin Metathesis and Natural Product Synthesis,” A. H. Hoveyda, S. J. Malcolmson, S. J. Meek, A. R. Zhugralin in Metathesis in Natural Product Synthesis; Cossy, J. Ed.; Wiley-VCH, 2010, 343, (Chapter 12).
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]30. “Catalytic Enantioselective Olefin Metathesis,” A. H. Hoveyda, S. J. Malcolmson, S. J. Meek, A. R. Zhugralin in Catalytic Asymmetric Synthesis; Ojima, I. Ed.; Wiley-VCH, 2010, 739 (Chapter 8E).
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]29. “Molybdenum,[(S)-3,3′-bis(1,1-dimethylethyl)-5,5′,6,6′-tetramethyl[1,1′-biphenyl]-2,2′-diolato(2-)-kO,kO’]-2-methyl-2-phenylpropylidene)[tricyclo[3.3.1.13,7]decan-1-aminato(2-)],” S. J. Malcolmson, A. H. Hoveyda, R. R. Schrock, (Encyclopedia of Reagents for Organic Synthesis, Second Edition; Paquette, Crich, Fuchs, Molander, Eds.; 1765-1768); Wiley-VCH: Weinheim, 2009.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]28. “The Remarkable Metal-catalysed Olefin Metathesis Reaction,” A. H. Hoveyda, A. R. Zhugralin Nature 2007, 450, 243.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]27. “Small Peptides as Ligands for Catalytic Asymmetric Alkylations of Olefins. Rational Design of Catalysts or of Searches that Lead to Them?,” A. H. Hoveyda, A. W. Hird, M. A. Kacprzynski Chem. Commun. 2004, 16, 1779.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]26. “Ru Complexes Bearing Bidentate Carbenes: From Innocent Curiosity to Uniquely Effective Catalysts for Olefin Metathesis,” A. H. Hoveyda, D. G. Gillingham, J. J. Van Veldhuizen, O. Kataoka, S. B. Garber, J. S. Kingsbury, J. P. A. Harrity Org. Biomol. Chem. 2004, 2, 8.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]25. “Combinatorial Approaches,” A. H. Hoveyda, K. E. Murphy in Comprehensive Asymmetric Catalysis, Supplement 1, E. N. Jacobsen, A. Pfaltz, H. Yamamoto, Eds.; Springer, 2004, 171 (Supplement to Chapter 39).
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]24. “Metathesis Reactions,” A. H. Hoveyda, R. R. Schrock in Comprehensive Asymmetric Catalysis, Supplement 1, E. N. Jacobsen, A. Pfaltz, H. Yamamoto, Eds.; Springer, 2004, 207 (Chapter 44).
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]23. “Molybdenum and Tungsten Imido Alkylidene Complexes as Efficient Olefin-Metathesis Catalysts,” R. R. Schrock, A. H. Hoveyda Angew. Chem., Int. Ed. Engl. 2003, 42, 4592.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]22. “Catalytic Asymmetric Olefin Metathesis,” A. H. Hoveyda, R. R. Schrock in Handbook of Metathesis, R. H. Grubbs, Ed.; VCH-Wiley, Weinhein, 2003, 128 (Vol. 2).
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]21. “Polymer-Supported Olefin Metathesis Catalysts for Organic and Combinatorial Synthesis,” J. S. Kingsbury and A. H. Hoveyda in Polymeric Materials in Organic Synthesis and Catalysis, M. R. Buchmeiser, Ed.; VCH-Wiley, Weinheim, 2003, 467.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]20. “Catalytic Asymmetric Olefin Metathesis,” A. H. Hoveyda in Organic Synthesis Highlights V, H-G. Schmalz and T. Wirth, Eds; VCH-Wiley, Weinheim, 2003, 210.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]19. “Chiral Zirconium Catalysts for Enantioselective Synthesis” A. H. Hoveyda in The Chemistry of Titanium and Zirconium Complexes, I. Marek, Ed.; VCH-Wiley, New York, 2002, 180.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]18. “Diversity-Based Approaches to Chiral Catalyst Discovery,” A. H. Hoveyda in The Handbook of Combinatorial Chemistry, K. C. Nicolaou, R. Hanko, W. Hartwig, Eds.; VCH-Wiley, Weinheim, 2002, 991.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]17. “Catalytic Asymmetric Olefin Metathesis,” A. H. Hoveyda, R. R. Schrock Chem. Eur. J. 2001, 7, 945.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]16. “High-Throughput Screening of Titanium-Tripeptide Schiff Base Complexes for Catalytic Asymmetric Addition of Trimethylsilylcyanide to Epoxides and Imines,” K. W. Kuntz, M. L. Snapper, A. H. Hoveyda in High-Throughput Synthesis, Sucholeiki, I., Ed.; Marcel Dekker: New York, 2000, 283.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]15. “Combinatorial Approaches to Chiral Catalyst Discovery,” M. L. Snapper and A. H. Hoveyda in Combinatorial Chemistry, Fenniri, H. Ed.; Oxford, 2000, 433.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]14. “Asymmetric Catalysis in Target-Oriented Synthesis,” A. H. Hoveyda in Stimulating Concepts in Chemistry, Stoddart, F. J., Shibasaki, M., Vogtle, F., Eds; VCH: Weinheim, 2000, 145.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]13. “Stereoselective Addition of Grignard Reagents to Alkenes,” A. H. Hoveyda, N. M. Heron, J. A. Adams in Grignard Reagents: New Developments, Richey, H. G., Ed.; John Wiley and Sons: New York, 2000, 107.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]12. “Combinatorial Catalysis: Identification of Potent Chiral Catalysts Through Fluorescent Bead Signaling,” A. H. Hoveyda Chem. & Biol. 1999, 6, R305.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]11. “Carbometallation of Carbon-Carbon Double Bonds,” A. H. Hoveyda, N. M. Heron in Comprehensive Asmmetric Catalysis, Vol. III, E. N. Jacobsen, A. Pfaltz, H. Yamamoto, Eds.; Springer-Verlag, 1999, 431.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]10. “Combinatorial Approaches,” K. D. Shimizu, M. L. Snapper, A. H. Hoveyda in Comprehensive Asmmetric Catalysis, E. N. Jacobsen, A. Pfaltz, H. Yamamoto, Eds.; Springer, 1999, 1389 (Chapter 39).
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]9. “Combinatorial Catalyst Discovery,” K. W. Kuntz, M. L. Snapper, A. H. Hoveyda Curr. Opinions in Chem. & Biol. 1999, 3, 313.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]8. “Metal-Catalyzed Kinetic Resolution Processes,” A. H. Hoveyda, M. T. Didiuk Curr. Org. Chem. 1998, 2, 489.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]7. “High-Throughput Strategies for the Discovery of Catalysts,” K. D. Shimizu, M. L. Snapper, A. H. Hoveyda Chem., Eur. J. 1998, 4, 1885.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]6. “Catalyst Discovery Through Combinatorial Chemistry,” A. H. Hoveyda Chemistry & Biology 1998, 5, R187.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]5. “Catalytic Ring-Closing Metathesis and the Development of Enantioselective Processes,” A. H. Hoveyda in Metathesis, Furstner, A., Ed.; Springer: Berlin, 1998, 105.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]4. “Chiral Titanocenes and Zirconocenes in Synthesis,” A. H. Hoveyda and J. P. Morken in Metallocenes, Togni, A.; Halterman R., Eds.; VCH: Weinheim; 1998, Vol. 2, 625.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]3. “Catalytic Enantioselective Addition of Grignard Reagents to Olefins,” A. H. Hoveyda in Transition Metals for Fine Chemicals and Organic Synthesis, Bolm, C. Ed.; VCH: Weinheim, 1998, 195.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]2. “Enantioselective C-C and C-H Bond Formation Mediated or Catalyzed by Chiral ebthi Complexes of Titanium and Zirconium,” A. H. Hoveyda, J. P. Morken Angew. Chem., Int. Ed. Engl. 1996, 35, 1263.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]1. “Substrate-Directable Chemical Reactions,” A. H. Hoveyda, D. A. Evans, G. C. Fu Chem. Rev. 1993, 93, 1307.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][/et_pb_column][/et_pb_row][/et_pb_section] [et_pb_section bb_built=”1″ module_id=”non-research” _builder_version=”4.0.3″ custom_margin=”-100px||||false|false” prev_background_color=”#000000″ next_background_color=”#000000″][et_pb_row _builder_version=”4.0.3″][et_pb_column type=”4_4″ _builder_version=”4.0.3″][et_pb_text _builder_version=”4.0.3″ header_3_text_color=”#e02b20″ custom_padding=”||0px|||”]NON-RESEARCH ARTICLES
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]2. “Primo Levi’s The Periodic Table. A Search for Patterns in Times Past,” A. H. Hoveyda, Angew. Chem., Int. Ed. Engl. 2004, 43, 6592.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]1. “Striving for Scientific Nirvana,” A. H. Hoveyda, Chemical & Engineering News 2001, 79, 198.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][/et_pb_column][/et_pb_row][/et_pb_section] [et_pb_section bb_built=”1″ module_id=”patents” _builder_version=”4.0.3″ custom_margin=”-100px||||false|false” prev_background_color=”#000000″][et_pb_row _builder_version=”4.0.3″][et_pb_column type=”4_4″ _builder_version=”4.0.3″][et_pb_text _builder_version=”4.0.3″ header_3_text_color=”#e02b20″ custom_padding=”||0px|||”]PATENTS
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]20. “Synthesis of Z-Alkenyl Halides Through Stereoselective Olefin Methathesis,” 2017, Patent Number US 9,850,268.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]19. “Z-Selective Ring-Closing Metathesis Reactions,” 2017, Patent Number US 9,771,386.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]18. “Catalysts for Efficient Z-Selective Metathesis,” 2017, Patent Number US 14,303,523.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]17. “Z-Selective Coupling of Terminal Olefins,” 2017, Patent Number US 9,713,808.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]16. “Unique Chiral-at-Metal Catalysts for Remarkably Efficient and Exceptionally Enantioslecetive Olefin Metathesis,” 2017, Patent Number US 9,687,834.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]15. “Z-Selective Ring-Closing Metathesis Reactions,” 2016, Patent Number US 9,446,394.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]14. “Tungsten Oxo Alkylidene Complexes for Z Selective Olefin Metathesis,” 2015, Patent Number US 9,085,595.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]13. “High Z-Selective Olefin Metathesis,” 2015, Patent Number US 9,079,173.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]12. “Simple Organic Molecules as Catalysts for Practical and Enantioselective Synthesis of Amines and Alcohols,” 2015, Patent Number US 2015/0057451.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]11. “Efficient Methods for Z– or cis-Selective Cross-Metathesis,” 2013, Patent Number US 8,598,400.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]10. “Highly Z-Selective Olefin Metathesis,” 2013, Patent Number US 8,362,311.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]9. “Complexes for Use in Metathesis Reactions,” 2013, Patent Number US 8,546,500.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]8. “Efficient Methods for Z– or cis-Selective Cross-Metathesis,” 2013, Patent Number US 8,552,242.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]7. “Catalysts and Processes for the Formation of Terminal Olefins by Ethenolysis,” 2012, Patent Number US 8,222,469.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]6. “Catalysts for Metathesis Including Enantioselective Olefin Metathesis, And Related Methods,” 2009, Patent Number International WO 2009/094201.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]5. “Recyclable Metathesis Catalysts,” 2010, Patent Number US 7,723,255.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]4. “Recyclable Metathesis Catalysts,” 2005, Patent Number US 6,921,735.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]3. “Recyclable Chiral Metathesis Catalysts,” 2005, Patent Number US 6,939,982.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]2. “Chiral Cyanoamines and Methods of Preparation,” 2004, Patent Number US 6,693,168.
[/et_pb_text][et_pb_divider color=”#cecece” _builder_version=”4.0.3″ custom_margin=”1px||1px||false|false” /][et_pb_text _builder_version=”4.0.3″]1. “Asymmetric Ring-Closing Metathesis Reactions Involving Achiral and Meso Substrates,” 2002, Patent Number US 6,346,652.
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