Zobrazeno 1 - 10
of 214
pro vyhledávání: '"Ol'ga A. Tarasova"'
Autor:
Boris A. Trofimov, Lubov’ N. Sobenina, Andrey P. Demenev, Al’bina I. Mikhaleva, Igor’ A. Ushakov, Ol’ga A. Tarasova, Vladimir I. Smirnov, Konstantin B. Petrushenko, Alexander I. Vokin, Natal’ya M. Murzina, Galina F. Myachina
Publikováno v:
ARKIVOC, Vol 2001, Iss 9, Pp 37-48 (2001)
Externí odkaz:
https://doaj.org/article/e1ef1077779142c987f2dbc0afd950ba
Autor:
Polina A. Shcherbo, Ol'ga D. Tarasova
Publikováno v:
Вестник Московского государственного областного университета, Iss 2 (2022)
Aim. A review of those morphological and syntactic features of incorporated complexes (IC) that allow them to become a means of speech compression.Methodology. The phenomenon of incorporation is studied from the point of view of morphological classif
Externí odkaz:
https://doaj.org/article/6ee86534cfd84412b8efdbe63be5e719
Autor:
Alexander V. Artem'ev, Evgeniya P. Doronina, Mariana I. Rakhmanova, Xiuze Hei, Dmitri V. Stass, Ol'ga A. Tarasova, Irina Yu. Bagryanskaya, Denis G. Samsonenko, Alexander S. Novikov, Nina A. Nedolya, Jing Li
Publikováno v:
Dalton Transactions. 52:4017-4027
We present 1D CuI-based polymers exhibiting remarkable short-lived TADF and phosphorescence induced by photo- or X-ray irradiation.
Autor:
Boris A. Trofimov, Ol'ga A. Tarasova, Marina A. Maximova, Alexander I. Albanov, Nina A. Nedolya
Publikováno v:
Synthesis. 54:2516-2526
Deprotonative metalation of N-isopropenyl-1H-pyrroles with superbases followed by trapping with a variety of electrophiles was studied as an effective tool for the regioselective functionalization of 1H-pyrroles.
Publikováno v:
Russian Journal of Organic Chemistry. 57:347-354
Fragmentation of 1-alkyl(cycloalkyl, alkoxyalkyl)-5-[(alkyl, allyl, benzyl)sulfanyl]-1H-pyrrol-2-amines under electron impact (70 eV) and chemical ionization (with methane as reactant gas) has been studied for the first time. All the examined compoun
Publikováno v:
Russian Journal of Organic Chemistry. 57:486-489
Successive one-pot reactions of monolithiated N,N-diethylprop-2-yn-1-amine with 2-(ethenyloxy)ethyl isothiocyanate and 2-(bromomethyl)-1,3-dioxolane afforded 5-[(1,3-dioxolan-2-ylmethyl)sulfanyl]-1[2-(ethenyloxy)ethyl]-N,N-diethyl-1H-pyrrol-2-amine
Publikováno v:
Russian Journal of Organic Chemistry. 57:287-291
The sequential reaction of lithiated methoxyallene, methyl isothiocyanate, and 2-(bromomethyl)-1,3-dioxolane in the presence of CuBr yields a 2,3-disubstituted thiophene instead of the expected pyrrole. The process is accomplished in one preparative
Publikováno v:
Russian Journal of Organic Chemistry. 57:283-286
An unusual [2+2]-cyclodimerization of 5-ethenylidene-4,5-dihydro-1,3-thiazole, obtained from lithiated methoxyallene, isopropyl isothiocyanate, and propargylbromide, into highly functionalized 1,3-bis(methylene)cyclobutane is discovered.
Publikováno v:
Proceedings of the International Scientific and Practical Conference "Sustainable development of environment after Covid-19" (SDEC 2021).
Publikováno v:
ChemistrySelect. 5:5726-5731