Vincent Gandon
Affiliations: | Organic | chemistry, Stony Brook, NY, United States |
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Sign in to add traineeManish Pareek | post-doc | 2017- | University of Paris-Sud, Orsay |
Sara P. Morcillo | post-doc | 2014-2016 | chemistry |
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Publications
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Naulin E, Lombard M, Gandon V, et al. (2023) Enantioselective and Regiodivergent Synthesis of Dihydro-1,2-oxazines from Triene-Carbamates via Chiral Phosphoric Acid-Catalysis. Journal of the American Chemical Society |
Sau S, Mukherjee K, Kondalarao K, et al. (2023) Probing Chiral Sulfoximine Auxiliaries in Ru(II)-Catalyzed One-Pot Asymmetric C-H Hydroarylation and Annulations with Alkynes. Organic Letters |
Wei J, Gandon V, Zhu Y. (2023) Amino Acid-Derived Ionic Chiral Catalysts Enable Desymmetrizing Cross-Coupling to Remote Acyclic Quaternary Stereocenters. Journal of the American Chemical Society |
Bhoyare VW, Sosa Carrizo ED, Chintawar CC, et al. (2023) Gold-Catalyzed Heck Reaction. Journal of the American Chemical Society. 145: 8810-8816 |
Chen Y, Gandon V, Bour C. (2022) Squaramide/Li-Catalyzed Direct S1-Type Reaction of Vinyl Triflates with Difluoroenoxysilanes through Vinyl Cations. Organic Letters |
Bera T, Singh B, Gandon V, et al. (2022) Experimental and Theoretical Investigation of an Azaoxyallyl Cation-Templated Intramolecular Aryl Amination Leading to Oxindole Derivatives. Chemistry (Weinheim An Der Bergstrasse, Germany) |
Yang S, Miaskiewicz S, Bour C, et al. (2022) Transition structures for the oxy-ene reaction. Chemical Communications (Cambridge, England) |
Dutta S, Shandilya S, Yang S, et al. (2022) Cationic-palladium catalyzed regio- and stereoselective syn-1,2-dicarbofunctionalization of unsymmetrical internal alkynes. Nature Communications. 13: 1360 |
Vanjari R, Dutta S, Yang S, et al. (2022) Palladium-Catalyzed Regioselective Arylalkenylation of Ynamides. Organic Letters. 24: 1524-1529 |
Han X, Gaignard-Gaillard Q, Retailleau P, et al. (2022) Synthesis of chiral polycyclic -heterocycles gold(I)-catalyzed 1,6-enyne cyclization/intramolecular nucleophilic addition. Chemical Communications (Cambridge, England) |