Zobrazeno 1 - 10
of 28
pro vyhledávání: '"N. E. Mysova"'
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
https://doi.org/10.1007/s11172-019-2558-4
Publikováno v:
Chemistry of Heterocyclic Compounds. 48:1634-1640
The mass spectrometric behavior of 1-alkyl-5-(1H-indol-2-yl)pyrrolidin-2-ones and 1-alkyl-5-(1H-indol-3-yl)pyrrolidin-2-ones was studied and the fragmentation of these compounds was established. The product of N-methylindole reaction with 1-benzyl-5-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::18a4e99e4cc374f5174e45bf688eb0a1
https://doi.org/10.1007/s10593-013-1185-5
https://doi.org/10.1007/s10593-013-1185-5
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
https://doi.org/10.1134/s1070428012030207
Autor:
N. E. Mysova, A. A. Ambartsumyan, Konstantin A. Kochetkov, T. T. Vasil’eva, O. V. Chakhovskaya
Publikováno v:
Russian Journal of Organic Chemistry. 50:752-754
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb0323498d9776235c701eaed1b781fc
https://doi.org/10.1134/s1070428014050236
https://doi.org/10.1134/s1070428014050236
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
https://doi.org/10.1134/s1070428009080119
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
https://doi.org/10.1016/j.jfluchem.2008.05.017
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
https://doi.org/10.1134/s1070428007040057
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
https://doi.org/10.1007/s11178-006-0007-y
Publikováno v:
Zeitschrift für anorganische und allgemeine Chemie. 631:2232-2235
The reaction of isoprene with aniline, catalyzed by Pd (acac)2–(RO)3P-CF3COOH, (1:4:4) (R = Me, Et, acac = (CH3CO)2CH-) in MeCN solution, results in high (up to 89 mol.%) selectivity of N–(3-methyl-2-buten-1-yl) aniline. The presence of telomeric
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6612ee16c1503874c3d8385c17b53625
https://doi.org/10.1002/zaac.200570049
https://doi.org/10.1002/zaac.200570049
Publikováno v:
Russian Journal of General Chemistry. 75:910-914
The reaction of isoprene with aniline, catalyzed by the Pd(acac)2-(RO)3P-CF3CO2H system, 1 : 4 : 4 [R = Me, Et; acac = (CH3CO)2CH], in MeCN provides N-(3-methylbut-2-en-1-yl)aniline with a high selectivity (up to 84%) and a nearly quantitative yield
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b531ce8be2eb91b8742755cec1b67003
https://doi.org/10.1007/s11176-005-0344-5
https://doi.org/10.1007/s11176-005-0344-5