Vladimir Gevorgyan, Ph.D.
Affiliations: | 1999-2019 | Chemistry | University of Illinois at Chicago, Chicago, IL, United States |
2019- | University of Texas at Dallas, Richardson, TX, United States |
Area:
Transition Metal CatalysisWebsite:
https://labs.utdallas.edu/gevorgyan-group/members/Google:
"Vladimir Gevorgyan"Bio:
https://profiles.utdallas.edu/vlad
Mean distance: 7.63 | S | N | B | C | P |
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Publications
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Zhang Z, Gevorgyan V. (2020) Co-Catalyzed Transannulation of Pyridotriazoles with Isothiocyanates and Xanthate Esters. Organic Letters |
Yadagiri D, Rivas M, Gevorgyan V. (2020) Denitrogenative Transformations of Pyridotriazoles and Related Compounds: Synthesis of -Containing Heterocyclic Compounds and Beyond. The Journal of Organic Chemistry. 85: 11030-11046 |
Gevorgyan V, Ratushnyy M, Kvasovs N, et al. (2020) Visible Light-Induced Palladium-Catalyzed Generation of Aryl Radicals from Aryl Triflates. Angewandte Chemie (International Ed. in English) |
Zhang Z, Yadagiri D, Gevorgyan V. (2019) Light-induced metal-free transformations of unactivated pyridotriazoles. Chemical Science. 10: 8399-8404 |
Kurandina D, Chuentragool P, Gevorgyan V. (2019) Transition-Metal-Catalyzed Alkyl Heck-Type Reactions. Synthesis. 51: 985-1005 |
Kurandina D, Yadagiri D, Rivas M, et al. (2019) Transition-Metal- and Light-Free Directed Amination of Remote Unactivated C(sp)-H Bonds of Alcohols. Journal of the American Chemical Society |
Gevorgyan V, Chuentragool P, Kurandina D. (2019) Catalysis by Visible Light Photoexcited Palladium Complexes. Angewandte Chemie (International Ed. in English) |
Gevorgyan V, Chuentragool P, Yadagiri D, et al. (2018) Aliphatic Radical Relay Heck Reaction at Unactivated C(sp3)-H Sites of Alcohols. Angewandte Chemie (International Ed. in English) |
Ratushnyy M, Kamenova M, Gevorgyan V. (2018) A mild light-induced cleavage of the S-O bond of aryl sulfonate esters enables efficient sulfonylation of vinylarenes. Chemical Science. 9: 7193-7197 |
Chuentragool P, Parasram M, Shi Y, et al. (2018) General, Mild, and Selective Method for Desaturation of Aliphatic Amines. Journal of the American Chemical Society |