Kin S. Yang, Ph.D.
Affiliations: | 2015-2016 | Chemistry | Scripps Research Institute, La Jolla, La Jolla, CA, United States |
| 2016- | Gilead |
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"Kin Yang"Parents
Sign in to add mentor| Donald C. Dittmer | research assistant | 2008-2010 | |
| Viresh H. Rawal | grad student | 2010-2015 | Chicago |
| Keary Mark Engle | post-doc | 2015- | Scripps Institute |
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Publications
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| Wang X, Li ZQ, Mai BK, et al. (2020) Controlling cyclization pathways in palladium(ii)-catalyzed intramolecular alkene hydro-functionalization substrate directivity. Chemical Science. 11: 11307-11314 |
| Romine AM, Yang KS, Karunananda MK, et al. (2019) Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis. Acs Catalysis. 9: 7626-7640 |
| Romine AM, Yang KS, Karunananda MK, et al. (2019) Synthetic and Mechanistic Studies of a Versatile Heteroaryl Thioether Directing Group for Pd(II) Catalysis Acs Catalysis. 9: 7626-7640 |
| Matsuura R, Jankins TC, Hill DE, et al. (2018) Palladium(ii)-catalyzed γ-selective hydroarylation of alkenyl carbonyl compounds with arylboronic acids. Chemical Science. 9: 8363-8368 |
| Tran VT, Gurak JA, Yang KS, et al. (2018) Activation of diverse carbon-heteroatom and carbon-carbon bonds via palladium(II)-catalysed β-X elimination. Nature Chemistry |
| Liu Z, Zeng T, Yang KS, et al. (2016) β,γ-Vicinal Dicarbofunctionalization of Alkenyl Carbonyl Compounds via Directed Nucleopalladation. Journal of the American Chemical Society |
| Yang KS, Gurak JA, Liu Z, et al. (2016) Catalytic, Regioselective Hydrocarbofunctionalization of Unactivated Alkenes with Diverse C-H Nucleophiles. Journal of the American Chemical Society |
| Yang KS, Engle KM. (2016) Organic chemistry: Precision pruning of molecules. Nature. 533: 183-184 |
| Gurak JA, Yang KS, Liu Z, et al. (2016) Directed, Regiocontrolled Hydroamination of Unactivated Alkenes via Protodepalladation. Journal of the American Chemical Society |
| Yang KS, Rawal VH. (2014) Synthesis of α-amino acid derivatives and peptides via enantioselective addition of masked acyl cyanides to imines. Journal of the American Chemical Society. 136: 16148-51 |