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Emmanuel A. Theodorakis research assistant 1998 UCSD
 (B.S.)
Larry E. Overman grad student 2004 UC Irvine
 (Investigation into the origins of diastereoselection in spirocyclic oxindole forming intramolecular Heck cyclizations.)
Robert G. Bergman post-doc 2004-2006 UC Berkeley
Stephen L. Buchwald post-doc 2006-2009 MIT
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Publications

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Kim RS, Kgoadi LO, Hayes JC, et al. (2024) Nickel-Catalyzed Atroposelective Cross-Electrophile Coupling of Aryl Halides: A General and Practical Route to Diverse MOP-Type Ligands. Journal of the American Chemical Society
Rezazadeh S, Martin MI, Kim RS, et al. (2023) Photoredox-Nickel Dual-Catalyzed -Alkylation of Secondary Nitroalkanes: Access to Sterically Hindered α-Tertiary Amines. Journal of the American Chemical Society
Pawley SB, Conner AM, Omer HM, et al. (2022) Development of a General Method for the Hiyama-Denmark Cross-Coupling of Tetrasubstituted Vinyl Silanes. Acs Catalysis. 12: 13108-13115
Korch KM, Watson DA. (2021) Total Synthesis of (±)-Impatien A via Aza-Heck Cyclization. Organic Letters
Gao RD, Shuler SA, Watson DA. (2021) Tandem aza-Heck Suzuki and carbonylation reactions of -phenyl hydroxamic ethers: complex lactams carboamination. Chemical Science. 12: 8859-8864
Idowu OO, Hayes JC, Reid WB, et al. (2021) Synthesis of 1,1-Diboryl Alkenes Using the Boryl-Heck Reaction. Organic Letters
Zuo Z, Kim RS, Watson DA. (2021) Synthesis of Axially Chiral 2,2'-Bisphosphobiarenes via a Nickel-Catalyzed Asymmetric Ullmann Coupling: General Access to Privileged Chiral Ligands without Optical Resolution. Journal of the American Chemical Society
Kim RS, Dinh-Nguyen LV, Shimkin KW, et al. (2020) Copper-Catalyzed Propargylation of Nitroalkanes. Organic Letters
Xu F, Duke OM, Rojas D, et al. (2020) Arylphosphonate-Directed Ortho C-H Borylation: Rapid Entry into Highly-Substituted Phosphoarenes. Journal of the American Chemical Society
Wisthoff MF, Pawley SB, Cinderella AP, et al. (2020) Stereoselective Synthesis of - and -Tetrasubstituted Vinyl Silanes Using a Silyl-Heck Strategy and Hiyama Conditions for Their Cross-Coupling. Journal of the American Chemical Society
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