Hongchao Zheng, Ph.D.
Affiliations: | Chemistry | University of Alberta, Edmonton, Alberta, Canada |
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"Hongchao Zheng"Mean distance: 8.57 | S | N | B | C | P |
Parents
Sign in to add mentor| Dennis G. Hall | grad student | 2012 | University of Alberta | |
| (Greener Chemistry Using Boronic Acids as Organocatalysts and Stoichiometric Reaction Promoters.) | ||||
| Michel R. Gagné | post-doc | 2012-2014 | UNC Chapel Hill | |
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Publications
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| Wang H, Shao Y, Zheng H, et al. (2015) Cyanoacetic Acid as a Masked Electrophile: Transition-Metal-Free Cyanomethylation of Amines and Carboxylic Acids. Chemistry (Weinheim An Der Bergstrasse, Germany) |
| Chen J, Shao Y, Zheng H, et al. (2015) Metal-Free Coupling of 2-Vinylphenols and Carboxylic Acids: An Access to 3-Acyloxy-2,3-Dihydrobenzofurans. The Journal of Organic Chemistry |
| Zheng H, Liu X, Xu C, et al. (2015) Regio- and Enantioselective Aza-Diels-Alder Reactions of 3-Vinylindoles: A Concise Synthesis of the Antimalarial Spiroindolone NITD609. Angewandte Chemie (International Ed. in English) |
| Zheng H, Adduci LL, Felix RJ, et al. (2014) Gold-catalyzed diastereoselective cycloisomerization of alkylidene-cyclopropane-bearing 1,6-diynes. Angewandte Chemie (International Ed. in English). 53: 7904-7 |
| Zheng H, Felix RJ, Gagné MR. (2014) Gold-catalyzed enantioselective ring-expanding cycloisomerization of cyclopropylidene bearing 1,5-enynes. Organic Letters. 16: 2272-5 |
| Gernigon N, Zheng H, Hall DG. (2013) Solid-supported ortho-iodoarylboronic acid catalyst for direct amidation of carboxylic acids Tetrahedron Letters. 54: 4475-4478 |
| Zheng H, Lejkowski M, Hall DG. (2013) Mild boronic acid catalyzed Nazarov cyclization of divinyl alcohols in tandem with Diels-Alder cycloaddition Tetrahedron Letters. 54: 91-94 |
| Zheng H, Lejkowski M, Hall DG. (2013) ChemInform Abstract: Mild Boronic Acid Catalyzed Nazarov Cyclization of Divinyl Alcohols in Tandem with Diels-Alder Cycloaddition. Cheminform. 44: no-no |
| Zheng H, Ghanbari S, Nakamura S, et al. (2012) Boronic acid catalysis as a mild and versatile strategy for direct carbo- and heterocyclizations of free allylic alcohols. Angewandte Chemie (International Ed. in English). 51: 6187-90 |
| Zheng H, Lejkowski M, Hall DG. (2011) Mild and selective boronic acid catalyzed 1,3-transposition of allylic alcohols and Meyer-Schuster rearrangement of propargylic alcohols Chemical Science. 2: 1305-1310 |