MH-Lab | Grigorii S. Astakhov

Grigorii S. Astakhov

Personal Info

Phone

+7-499-135-93-69

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Academic Degree

Master of Science

Experience

Master degree (2017, RUDN University):2017-present: PhD Student

Scientific Interests

Cage-like compounds of transition metals, complexation reactions, synthesis of heterocyclic compounds: domino-, multi-step and one-top reactions

Publications

2022

Crystal Growth and Design, 2022, 22(4), 2146-2157, DOI: 10.1021/acs.cgd.1c01225
A. N. Bilyachenko, G. S. Astakhov, A. N. Kulakova, Korlyukov Alexander A., Zubavichus Yan V., Dorovatovskii Pavel V., Shul’pina Lidia S., E. S. Shubina, Ikonnikov Nikolay S., Kirillova Marina V., Zueva Anna Y., Kirillov Alexander M., G. B. Shul’pin
Exploring Cagelike Silsesquioxane Building Blocks for the Design of Heterometallic Cu4/M4 Architectures

2021

Inorg. Chem., 2021, 60(11), 8062-8074, DOI: 10.1021/acs.inorgchem.1c00586
G. S. Astakhov, M. M. Levitsky, Zubavichus Y. V., Khrustalev Victor N., A. A. Titov, Dorovatovskii Pavel V., Smol’yakov Alexander F., E. S. Shubina, Kirillova Marina V., A. Kirillov, A. N. Bilyachenko
Cu6- and Cu8-Cage Sil- and Germsesquioxanes: Synthetic and Structural Features, Oxidative Rearrangements, and Catalytic Activity

2020

J. Organomet. Chem., 2020, 906, DOI: 10.1016/j.jorganchem.2019.121022
G. S. Astakhov, M. M. Levitsky, Bantreil X., F. Lamaty, Khrustalev V.N., Zubavichus Y.V., Dorovatovskii P.V., E. S. Shubina, A. N. Bilyachenko
Cu(II)-silsesquioxanes as efficient precatalysts for Chan-Evans-Lam coupling
Inorg. Chem., 2020, 59(7) , 4536–4545, DOI: 10.1021/acs.inorgchem.9b03680
G. S. Astakhov, A. N. Bilyachenko, M. M. Levitsky, Lidia S. Shulpina, Alexander A. Korlyukov, Yan V. Zubavichus, Victor N. Khrustalev, Anna V. Vologzhanina, E. S. Shubina, Pavel V. Dorovatovskii, G. B. Shul’pin
Coordination Affinity of Cu(II)-Based Silsesquioxanes toward N,N-Ligands and Associated Skeletal Rearrangements: Cage and Ionic Products Exhibiting a High Catalytic Activity in Oxidation Reactions

2019

J. Organomet. Chem., 2019, DOI: 10.1016/j.jorganchem.2019.121022
G. S. Astakhov, M. M. Levitsky, X. Bantreil, F. Lamaty, V.N. Khrustalev, Y.V. Zubavichus, P.V. Dorovatovskii, E. S. Shubina, A. N. Bilyachenko
Cu(II)-silsesquioxanes as efficient precatalysts for Chan-Evans-Lam coupling
Catalysts, 2019, 9(9), 701-719, DOI: 10.3390/catal9090701
G. S. Astakhov, M. M. Levitsky, A. A. Korlyukov, L. S. Shul’pina, E. S. Shubina, N. S. Ikonnikov, A. V. Vologzhanina, A. N. Bilyachenko, P. V. Dorovatovskii, Y. N. Kozlov, G. B. Shul’pin
New Cu4Na4- and Cu5-Based Phenylsilsesquioxanes. Synthesis via Complexation with 1,10-Phenanthroline, Structures and High Catalytic Activity in Alkane Oxidations with Peroxides in Acetonitrile

2018

Crystal Growth and Design, 2018, 18(9), 5377–5384, DOI: 10.1021/acs.cgd.8b00778
G. S. Astakhov, A. N. Bilyachenko, M. M. Levitsky, A.A. Korlyukov, Y.V. Zubavichus, P.V. Dorovatovskii, V.N. Khrustalev, A.V. Vologzhanina, E. S. Shubina
Tridecanuclear CuII11Na2 cagelike silsesquioxanes
Inorg. Chem., 2018, 57 (18), 11524–11529, DOI: 10.1021/acs.inorgchem.8b01496
G. S. Astakhov, A. N. Bilyachenko, A. Korlyukov, M. M. Levitsky, L. Shul'pina, X. Bantreil, F. Lamaty, A. Vologzhanina, E. S. Shubina, P. Dorovatovskii, D. Nesterov, A. Pombeiro, G. B. Shul’pin
High cluster (Cu9) cage silsesquioxanes. Synthesis, structure and catalytic activity

2017

Synthesis, 2017, 49(23), 5251-5257, DOI: 10.1055/s-0036-1588486
M. D. Matveevaa, T. N. Borisova, A. A. Titov, L. V. Anikina, S. V. Dyachenko, G. S. Astakhov, A. V. Varlamov, L. G. Voskressensky
Domino reactions of 1-aroyl-3,4-dihydroisoquinolines with ,-unsaturated aldehydes