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Anton Kozyryev
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Features of two-and multicomponent heterocyclization reactions involving 3, 4-disubstituted 5-aminopyrazoles and alkyl pyruvates
YI Sakhno, AV Kozyryev, SM Desenko, SV Shishkina, VI Musatov, ...
Tetrahedron 74 (5), 564-571, 2018
142018
Heterocyclization reactions of pyruvic acids and aminoazoles with controlled chemoselectivity
Y Sakhno, M Murlykina, A Morozova, A Kozyrev, V Chebanov
French-Ukrainian Journal of Chemistry 3 (2), 1-20, 2015
142015
Ultrasonic-assisted unusual four-component synthesis of 7-azolylamino-4, 5, 6, 7-tetrahydroazolo [1, 5-a] pyrimidines
YI Sakhno, MV Murlykina, OI Zbruyev, AV Kozyryev, SV Shishkina, ...
Beilstein Journal of Organic Chemistry 16 (1), 281-289, 2020
102020
Substrate electronics dominate the rate of reductive dehalogenation promoted by the flavin-dependent iodotyrosine deiodinase
A Kozyryev, D Lemen, J Dunn, SE Rokita
Biochemistry 62 (7), 1298-1306, 2023
42023
19F NMR Reveals the Dynamics of Substrate Binding and Lid Closure for Iodotyrosine Deiodinase as a Complement to Steady-State Kinetics and Crystallography
HC Greenberg, A Majumdar, EK Cheema, A Kozyryev, SE Rokita
Biochemistry 63 (17), 2225-2232, 2024
32024
The 2′-hydroxy group of flavin mononucleotide influences the catalytic function and promiscuity of the flavoprotein iodotyrosine dehalogenase
A Kozyryev, PA Boucher, CM Quiñones-Jurgensen, SE Rokita
RSC Chemical Biology 4 (9), 698-705, 2023
22023
A SEARCH FOR THE RATE DETERMINING STEP OF IODOTYROSINE DEIODINASE CATALYSIS AND MINIMAL REQUIREMENT FOR ENZYME CATALYZED DEIODINATION
A Kozyryev
Johns Hopkins University, 2021
2021
The Importance of a Phenolic Group in the Substrates of Iodotyrosine Deiodinase
CM Quinones, A Kozyryev, S Rokita
The FASEB Journal 32, 796.13-796.13, 2018
2018
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