Kin S. Yang, Ph.D.

2015-2016 Chemistry Scripps Research Institute, La Jolla, La Jolla, CA, United States 
 2016- Gilead 
"Kin Yang"
Mean distance: 7.58


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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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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
Yang KS, Nibbs AE, Türkmen YE, et al. (2013) Squaramide-catalyzed enantioselective Michael addition of masked acyl cyanides to substituted enones. Journal of the American Chemical Society. 135: 16050-3
Yang KS, Hudson B. (2010) Computation of deuterium isotope perturbation of 13C NMR chemical shifts of alkanes: a local mode zero-point level approach. The Journal of Physical Chemistry. A. 114: 12283-90
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