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Yun He, Ph.D.

Affiliations: 
Scripps Research Institute, La Jolla, La Jolla, CA, United States 
Area:
chemistry, biology, and medicine of natural and designed molecules
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"Yun He"
Mean distance: 7.92
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K. C. Nicolaou grad student 2000 Scripps Institute
 (Total synthesis and biological evaluation of epothilones.)

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Publications

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Geng S, Zhang J, Chen S, et al. (2020) Development and Mechanistic Studies of Iron-Catalyzed Construction of Csp-B Bonds via C-O Bond Activation. Organic Letters
Zhao S, Zang ZL, Li S, et al. (2020) Iridium-Catalyzed Cycloisomerization of N-Tethered 1,7-Enynes: Construction of Azabicyclo [5.1.0] octene System. The Journal of Organic Chemistry
Mao CL, Zhao S, Zang ZL, et al. (2019) Pd-Catalyzed remote site- and stereo-selective C(alkenyl)-H alkenylation of unactivated cycloalkenes. The Journal of Organic Chemistry
Lagishetti C, Banne S, You H, et al. (2019) Construction of Bridged-Ring-Fused Naphthalenone Derivatives Through an Unexpected Zn(OTf)-Catalyzed Cascade Transformation. Organic Letters
Allu SR, Banne S, Jiang J, et al. (2019) A Unified Synthetic Approach to Optically Pure Curvularin-type Metabolites. The Journal of Organic Chemistry
Liu Y, Wang Z, Banne S, et al. (2019) Towards the Total Synthesis of Scabrosins: Synthesis of Desulfur-scabrosins Skeleton and Its Stereoisomers. The Journal of Organic Chemistry
Wu Q, Shao P, He Y. (2019) Synthesis of 1,4,5,6-tetrahydropyridazines and pyridazines via transition-metal-free (4 + 2) cycloaddition of alkoxyallenes with 1,2-diaza-1,3-dienes Rsc Advances. 9: 21507-21512
Lin Z, Xu X, Zhao S, et al. (2018) Total synthesis and antimicrobial evaluation of natural albomycins against clinical pathogens. Nature Communications. 9: 3445
Addepalli Y, Yu Z, Ji J, et al. (2018) Tandem Diels-Alder/oxidation-aromatization reactions involving 2-styrylchromones and arynes. Organic & Biomolecular Chemistry
Zhang N, Yu Z, Yang X, et al. (2018) Difuran-substituted quinoxalines as a novel class of PI3Kα H1047R mutant inhibitors: Synthesis, biological evaluation and structure-activity relationship. European Journal of Medicinal Chemistry. 157: 37-49
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