Zobrazeno 1 - 10 of 119 pro vyhledávání: '"T. T. Vasil′eva"'
1
The use of iron carbonyls in the C—C bond formation reactions
Autor: N. E. Mysova, T. T. Vasil′eva, Konstantin A. Kochetkov, R. G. Gasanov, N. A. Bystrova
Publikováno v: Russian Chemical Bulletin. 68:1301-1320
The review systematizes material by key types of reactions promoted by iron carbonyls. The reaction types are subdivided into several principal directions, focusing mainly on new examples where iron carbonyls are used in the synthetically valuable C
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5ab472d7eb3d95a476c49d342517b1e4
https://doi.org/10.1007/s11172-019-2558-4
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2
Aza-Michael reaction as an efficient method for the synthesis of first representatives of β-azahetaryl-β-diphenylphosphorylalkanones
Autor: E. I. Goryunov, Polina S. Protopopova, M. A. Galkina, Konstantin A. Kochetkov, I. B. Goryunova, Valery K. Brel, A. B. Uryupin, T. T. Vasil'eva, G. V. Bodrin, A. E. Saifutiarova, Asmik A. Ambartsumyan
Publikováno v: Russian Chemical Bulletin. 65:1855-1858
Aza-Michael reaction of (E)-4-(diphenylphosphoryl)but-3-en-2-one (1) with a number of mono-and bicyclic nitrogen heterocycles proceeds regioselectively in the absence of catalysts with the formation of corresponding β-azahetaryl β-diphenylphosphory
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d966a8725da2a9bac8dede7dd3c47dcd
https://doi.org/10.1007/s11172-016-1520-y
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4
Transformations of 4-oxo-4H-chromene-3-carbaldehyde under the action of Fe(CO)5
Autor: Vladislav A. Tuskaev, T. T. Vasil’eva, A. A. Ambartsumyan, N. E. Mysova, O. V. Chakhovskaya, Victor N. Khrustalev, Konstantin A. Kochetkov
Publikováno v: Russian Journal of Organic Chemistry. 48:451-455
Transformations of 4-oxo-4H-chromene-3-carbaldehyde in the presence of pentacarbonyliron and HMPA in benzene and toluene were studied, and their probable mechanism was proposed. The structure of 3-(4-oxochroman-3-ylmethyl)-4H-chromen-4-one was determ
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::261692330de287f4cd55353438889669
https://doi.org/10.1134/s1070428012030207
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6
Benzyl bromide addition to pentafluorobenzaldehyde by Zaitsev-Barbier reaction promoted with complex systems underlain by iron pentacarbonyl
Autor: O. V. Chakhovskaya, T. T. Vasil'eva, N. E. Mysova, Konstantin A. Kochetkov, A. A. Ambartsumyan, A. B. Terent'ev
Publikováno v: Russian Journal of Organic Chemistry. 45:1181-1184
Iron pentacarbonyl promots addition of benzyl bromide to benzaldehydes by Zaitsev-Barbier reaction only in the presence of nucleophilic additives [HMPT or (S)-N-benzoyl-2-methoxycarbonylpyrrolidine].
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2d15ac133c51bd80dc947ab898378f14
https://doi.org/10.1134/s1070428009080119
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7
Pentafluorophenyl carbonyl compounds in the Reformatsky-type reactions promoted with Fe(CO)5-based metal complex systems
Autor: A. B. Terent'ev, O. V. Chahovskaya, Konstantin A. Kochetkov, T. T. Vasil'eva, H. H. Hambardzumyan, N. E. Mysova
Publikováno v: Journal of Fluorine Chemistry. 129:669-673
Iron pentacarbonyl is an effective promoter for additions of halogenated acid esters and nitriles to pentafluorophenyl carbonyl compounds 1 , 4 , and 5 by the Reformatsky-type reaction and reductive coupling of compound 1 . The electron-withdrawing c
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::7ca3a8c6edef69ef7693e39c8d486a5e
https://doi.org/10.1016/j.jfluchem.2008.05.017
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8
Diastereoselective synthesis of pinacols from aromatic aldehydes using the system pentacarbonyliron-hexamethylphosphoric triamide. Dual reactivity of pentafluorobenzaldehyde
Autor: A. B. Terent'ev, T. T. Vasil’eva, Konstantin A. Kochetkov, O. V. Chakhovskaya, N. E. Mysova
Publikováno v: Russian Journal of Organic Chemistry. 43:518-521
The system Fe(CO)5-HMPA effectively promotes diastereoselective reductive dimerization of aromatic aldehydes to the corresponding pinacols having preferentially or exclusively dl configuration. In the reaction with pentafluorobenzaldehyde, the produc
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::09ce1612ecf1ec1fa3160b9f501e4dff
https://doi.org/10.1134/s1070428007040057
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9
Addition of Halocarboxylic Acids Esters and Halohydrocarbons to Pentafluorobenzaldehyde Promoted by Iron Pentacarbonyl
Autor: O. V. Chakhovskaya, A. B. Terent'ev, Konstantin A. Kochetkov, T. T. Vasil’eva, N. E. Mysova
Publikováno v: Russian Journal of Organic Chemistry. 41:1615-1618
Iron pentacarbonyl is an efficient promoter of addition to the carbonyl group of pentafluorobenzene of alkyl α-halocarboxylates and alkyl halides. The electron-acceptor character of the pentafluorophenyl group essentially affects the course of react
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::3442f9a3888f25ffd4b6e71bb2653221
https://doi.org/10.1007/s11178-006-0007-y
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10
Addition of α-Halo-substituted Carbonitriles to and AldehydesKetones in the Presence of Iron Pentacarbonyl
Autor: A. B. Terent'ev, N. A. Kuz'mina, T. T. Vasil’eva, N. E. Mysova, O. V. Chakhovskaya
Publikováno v: Russian Journal of Organic Chemistry. 40:174-177
Halo-substituted carbonitriles in the presence of iron pentacarbonyl react with aldehydes and ketones by Reformatsky reaction type. In contract to halo-substituted esters the nitriles are considerably more reactive toward ketones than aldehydes. At t
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::716b8e9461f560557aec64494bcba3c9
https://doi.org/10.1023/b:rujo.0000034937.39138.2a
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