Нечаев Михаил Сергеевич
Нечаев Михаил Сергеевич
Академические должности
Должность
Организационная структура
Дата активности
Должность
отделение почётного звания
Профиль
Научные интересы
Металлоорганическая химия, гомогенный катализ, квантово-химическое моделирование
Научные публикации
Kolychev, E.L., Portnyagin, I.A., Shuntikov, V.V., Khrustalev, V.N., Nechaev, M.S. Six- and seven-membered ring carbenes: Rational synthesis of amidinium salts, generation of carbenes, synthesis of Ag(I) and Cu(I) complexes. (2009) Journal of Organometallic Chemistry, 694 (15), pp. 2454-2462. DOI: 10.1016/j.jorganchem.2009.03.014
Kolychev, E.L., Asachenko, A.F., Dzhevakov, P.B., Bush, A.A., Shuntikov, V.V., Khrustalev, V.N., Nechaev, M.S. Expanded ring diaminocarbene palladium complexes: Synthesis, structure, and Suzuki-Miyaura cross-coupling of heteroaryl chlorides in water. (2013) Dalton Transactions, 42 (19), pp. 6859-6866. DOI: 10.1039/c3dt32860k
Tukov, A.A., Normand, A.T., Nechaev, M.S. N-heterocyclic carbenes bearing two, one and no nitrogen atoms at the ylidene carbon: Insight from theoretical calculations. (2009) Dalton Transactions, (35), pp. 7015-7028. DOI: 10.1039/b906969k
Morozov, O.S., Lunchev, A.V., Bush, A.A., Tukov, A.A., Asachenko, A.F., Khrustalev, V.N., Zalesskiy, S.S., Ananikov, V.P., Nechaev, M.S. Expanded-ring N-heterocyclic carbenes efficiently stabilize gold(I) cations, leading to high activity in π-acid-catalyzed cyclizations. (2014) Chemistry - A European Journal, 20 (20), pp. 6162-6170. DOI: 10.1002/chem.201303760
Normand, A.T., Nechaev, M.S., Cavell, K.J. Mechanisms in the reaction of palladium(II)-π-Allyl complexes with aryl halides: Evidence for NHC exchange between two palladium complexes. (2009) Chemistry - A European Journal, 15 (29), pp. 7063-7073. DOI: 10.1002/chem.200900373
Chesnokov, G.A., Topchiy, M.A., Dzhevakov, P.B., Gribanov, P.S., Tukov, A.A., Khrustalev, V.N., Asachenko, A.F., Nechaev, M.S. Eight-membered-ring diaminocarbenes bearing naphthalene moiety in the backbone: DFT studies, synthesis of amidinium salts, generation of free carbene, metal complexes, and solvent-free copper catalyzed azide-alkyne cycloaddition (CuAAC) reaction. (2017) Dalton Transactions, 46 (13), pp. 4331-4345. DOI: 10.1039/c6dt04484k
Ageshina, A.A., Chesnokov, G.A., Topchiy, M.A., Alabugin, I.V., Nechaev, M.S., Asachenko, A.F. Making endo-cyclizations favorable again: A conceptually new synthetic approach to benzotriazoles via azide group directed lithiation/cyclization of 2-azidoaryl bromides. (2019) Organic and Biomolecular Chemistry, 17 (18), pp. 4523-4534. DOI: 10.1039/c9ob00615j
Nechaev, M.S. Tetrylenes: Electronic Structure, Stability, Reactivity, and Ligand Properties - A Comparative DFT Study. (2021) Organometallics, 40 (20), pp. 3408-3423. DOI: 10.1021/acs.organomet.1c00440
Премии и награды
Премия имени И.И. Шувалова Московского университета за научные работы, 2013
Премия Правительства Москвы молодым ученым, 2016
Персональные профили исследователя
Web of Science: K-6580-2012
Scopus: 6602092575
РИНЦ:
ORCID: 0000-0001-8941-4856
MathSciNet: