Hengbin Wang, Ph.D.
Affiliations: | 2012 | Chemistry | Emory University, Atlanta, GA |
Area:
synthesis of biologically active natural productsGoogle:
"Hengbin Wang"Mean distance: 9.59
Parents
Sign in to add mentorHuw M. L. Davies | grad student | 2012 | Emory | |
(Synthesis of cyclopropanes and dihydrofurans by metal carbenoid reactions.) |
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Publications
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Vogt DB, Seath CP, Wang H, et al. (2019) Selective C-F Functionalization of Unactivated Trifluoromethylarenes. Journal of the American Chemical Society |
Gilbert MM, DeMars MD, Yang S, et al. (2017) Synthesis of Diverse 11- and 12-Membered Macrolactones from a Common Linear Substrate Using a Single Biocatalyst. Acs Central Science. 3: 1304-1310 |
Wang H, Jui NT. (2017) Catalytic Defluoroalkylation of Trifluoromethylaromatics with Unactivated Alkenes. Journal of the American Chemical Society |
Wang H, Lu G, Sormunen GJ, et al. (2017) NHC Ligands Tailored for Simultaneous Regio- and Enantiocontrol in Nickel-Catalyzed Reductive Couplings. Journal of the American Chemical Society |
Aycock RA, Wang H, Jui NT. (2017) A mild catalytic system for radical conjugate addition of nitrogen heterocycles. Chemical Science. 8: 3121-3125 |
Li X, Wang H, Schneider JA, et al. (2017) Catalyst-free one-step synthesis of ortho-tetraaryl perylene diimides for efficient OPV non-fullerene acceptors Journal of Materials Chemistry C. 5: 2781-2785 |
Jackson EP, Malik HA, Sormunen GJ, et al. (2015) Mechanistic Basis for Regioselection and Regiodivergence in Nickel-Catalyzed Reductive Couplings. Accounts of Chemical Research. 48: 1736-45 |
Wang H, Negretti S, Knauff AR, et al. (2015) Exo-selective reductive macrocyclization of ynals. Organic Letters. 17: 1493-6 |
Lu P, Mailyan A, Gu Z, et al. (2014) Enantioselective synthesis of (-)-maoecrystal V by enantiodetermining C-H functionalization. Journal of the American Chemical Society. 136: 17738-49 |
Fu L, Wang H, Davies HM. (2014) Role of ortho-substituents on rhodium-catalyzed asymmetric synthesis of β-lactones by intramolecular C-H insertions of aryldiazoacetates. Organic Letters. 16: 3036-9 |