Chunhui Huang

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2007-2012 Chemistry University of Illinois at Chicago, Chicago, IL, United States 
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"Chunhui Huang"
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Vladimir Gevorgyan grad student 2007-2012 University of Illinois, Chicago
 (Temporary Silicon Tether Strategy for Palladium-Catalyzed Carbon-Hydrogen Activation Reactions.)
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Ghavtadze N, Melkonyan FS, Gulevich AV, et al. (2014) Conversion of 1-alkenes into 1,4-diols through an auxiliary-mediated formal homoallylic C-H oxidation. Nature Chemistry. 6: 122-5
Huang C, Ghavtadze N, Godoi B, et al. (2012) Pd-catalyzed modifiable silanol-directed aromatic C-H oxygenation. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 9789-92
Huang C, Chernyak N, Dudnik AS, et al. (2011) The Pyridyldiisopropylsilyl Group: A Masked Functionality and Directing Group for Monoselective ortho-Acyloxylation and ortho-Halogenation Reactions of Arenes. Advanced Synthesis & Catalysis. 353
Huang C, Giokaris A, Gevorgyan V. (2011) Palladium-Catalyzed Highly Regioselective C-3 Arylation of Imidazo[1,5-a]pyridine. Chemistry Letters. 40
Huang C, Ghavtadze N, Chattopadhyay B, et al. (2011) Synthesis of catechols from phenols via Pd-catalyzed silanol-directed C-H oxygenation. Journal of the American Chemical Society. 133: 17630-3
Huang C, Chattopadhyay B, Gevorgyan V. (2011) Silanol: a traceless directing group for Pd-catalyzed o-alkenylation of phenols. Journal of the American Chemical Society. 133: 12406-9
Dudnik AS, Chernyak N, Huang C, et al. (2010) A general strategy toward aromatic 1,2-ambiphilic synthons: palladium-catalyzed ortho-halogenation of PyDipSi-arenes. Angewandte Chemie (International Ed. in English). 49: 8729-32
Chernyak N, Dudnik AS, Huang C, et al. (2010) PyDipSi: a general and easily modifiable/traceless Si-tethered directing group for C-H acyloxylation of arenes. Journal of the American Chemical Society. 132: 8270-2
Huang C, Gevorgyan V. (2010) Synthesis of unsymmetrical o-biphenols and o-binaphthols via silicon-tethered Pd-catalyzed C-H arylation. Organic Letters. 12: 2442-5
Huang C, Gevorgyan V. (2009) TBDPS and Br-TBDPS protecting groups as efficient aryl group donors in Pd-catalyzed arylation of phenols and anilines. Journal of the American Chemical Society. 131: 10844-5
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