Guoting Zhang

Affiliations: 
École Polytechnique Fédérale de Lausanne, Lausanne, Switzerland 
Area:
organic chemistry
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"Guoting Zhang"
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Parents

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Aiwen Lei grad student 2013-2015 Wuhan University
Nicolai Cramer post-doc 2021-
Barry M. Trost post-doc 2018-2021 Stanford
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Publications

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Trost BM, Zhang G, Xu M, et al. (2021) ProPhenol Derived Ligands to Simultaneously Coordinate a Main Group-Metal and a Transition Metal: Application to a Zn-Cu Catalyzed Reaction. Chemistry (Weinheim An Der Bergstrasse, Germany)
Trost BM, Zhang G, Gholami H, et al. (2021) Total Synthesis of Kadcoccinic Acid A Trimethyl Ester. Journal of the American Chemical Society
Trost BM, Cregg JJ, Hohn C, et al. (2020) Ruthenium-catalysed multicomponent synthesis of the 1,3-dienyl-6-oxy polyketide motif. Nature Chemistry
Hu X, Nie L, Zhang G, et al. (2020) Electrochemical Oxidative [4+2] Annulation for the π-Extension of Unfunctionalized Hetero-biaryl Compounds. Angewandte Chemie (International Ed. in English)
Trost BM, Zhang G. (2020) Ruthenium-catalyzed Intermolecular Coupling of Vinylic 1,2-Bisboronates with Alkynes: Stereoselective Access to Boryl-Substituted Homoallylic Alcohols. Journal of the American Chemical Society
Hu X, Zhang G, Nie L, et al. (2019) Electrochemical oxidation induced intermolecular aromatic C-H imidation. Nature Communications. 10: 5467
Zhang L, Zhang G, Wang P, et al. (2018) Electrochemical Oxidation with Lewis-Acid Catalysis Leads to Trifluoromethylative Difunctionalization of Alkenes Using CFSONa. Organic Letters
Zhang L, Zhang G, Li Y, et al. (2018) The synergistic effect of self-assembly and visible-light induced the oxidative C-H acylation of N-heterocyclic aromatic compounds with aldehydes. Chemical Communications (Cambridge, England)
Hu X, Zhang G, Bu F, et al. (2018) Photoinduced oxidative activation of electron-rich arenes: alkenylation with H evolution under external oxidant-free conditions. Chemical Science. 9: 1521-1526
Zhang G, Lin Y, Luo X, et al. (2018) Oxidative [4+2] annulation of styrenes with alkynes under external-oxidant-free conditions. Nature Communications. 9: 1225
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