Zobrazeno 1 - 10
of 41
pro vyhledávání: '"V. A. Ferapontov"'
Publikováno v:
Russian Chemical Bulletin. 64:859-863
5-R-Pyrrolidin-2-ones were synthesized by Pd/Sibunit-catalyzed C—O hydrogenolysis of 5-R-5-hydroxypyrrolidin-2-ones with molecular hydrogen.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::21839141a027fb1f9b074de78a73278f
https://doi.org/10.1007/s11172-015-0945-z
https://doi.org/10.1007/s11172-015-0945-z
Autor:
V. A. Ferapontov, O. V. Turova, Maxim G. Vinogradov, E. V. Starodubtseva, Marina I. Struchkova
Publikováno v:
Tetrahedron: Asymmetry. 20:2121-2124
The catalytic asymmetric hydrogenation of acylsuccinates using RuCl3 as a precatalyst and atropisomeric diphosphines as chiral auxiliaries allows the synthesis of optically active 2-alkylparaconic acid esters in preparative yields with enantioselecti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cc3d3ae74ed7a06558f43b09f36bc40a
https://doi.org/10.1016/j.tetasy.2009.09.006
https://doi.org/10.1016/j.tetasy.2009.09.006
Publikováno v:
Journal of Molecular Catalysis A: Chemical. 311:61-65
The kinetics of asymmetric hydrogenation of methyl levulinate in the presence of the (COD)Ru(2-methylallyl)2–BINAP–HCl catalytic system was studied. The kinetic order in H2, as well as in the catalyst, was found to be equal to 1, whereas the kine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ecbc040b75c0c792413e34bc72062edb
https://doi.org/10.1016/j.molcata.2009.06.024
https://doi.org/10.1016/j.molcata.2009.06.024
Autor:
Marina I. Struchkova, V. A. Ferapontov, L. S. Gorshkova, O. V. Turova, Maxim G. Vinogradov, E. V. Starodubtseva
Publikováno v:
Tetrahedron. 64:11713-11717
A convenient one-step synthesis of chiral γ-lactones has been performed. The method is based on enantioselective hydrogenation of γ-ketoesters using the RuCl 3 –BINAP–HCl catalytic system. Chiral γ-lactones (91–99% ee) have been isolated in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::11b2c889f21df76766800dfab17e9b55
https://doi.org/10.1016/j.tet.2008.10.012
https://doi.org/10.1016/j.tet.2008.10.012
Publikováno v:
Russian Chemical Bulletin. 54:2374-2378
The rate of hydrogenation of γ-ketoesters MeCOCH2CH2COOR (R = Et, Pri, But) in the presence of the chiral RuII—BINAP catalyst (BINAP is 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl) greatly increases upon the addition of 5–10 equivalents of H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c685c2735d9f77892b0ff827001d994
https://doi.org/10.1007/s11172-006-0125-2
https://doi.org/10.1007/s11172-006-0125-2
Autor:
G. V. Chel'tsova, G. L. Heise, V. A. Ferapontov, D. V. Kurilov, O. V. Shishk, Maxim G. Vinogradov, L. S. Gorshkova
Publikováno v:
Russian Chemical Bulletin. 52:1841-1846
An improved procedure was developed for asymmetric reduction of acetophenone and propiophenone by the chiral reagent NaAl(IPTOLate)H2. This procedure is based on isolation of the chiral alcohol that formed as a crystalline host—guest complex with t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::45b0ed1b96c21f60f443451bdaed0961
https://doi.org/10.1023/a:1026117026241
https://doi.org/10.1023/a:1026117026241
Autor:
G. L. Heise, V. A. Ferapontov, L. S. Gorshkova, I. V. Razmanov, V. A. Pavlov, Maxim G. Vinogradov, G. V. Chel\\'tsova, O. R. Malyshev
Publikováno v:
Russian Chemical Bulletin. 52:471-479
Prochiral substrates (alkyl aryl ketones, cyclopropyl methyl ketone, 1-indanone, 1-tetralone, ethyl 2-oxo-4-phenylbutyrate, and N-(diphenylphosphinyl)acetophenoneimine) were subjected to asymmetric reduction with aluminum hydride reagents, which were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c09be8536ba67c5cac908c7d740ba781
https://doi.org/10.1023/a:1023443807540
https://doi.org/10.1023/a:1023443807540
Autor:
E. V. Starodubtseva, Maxim G. Vinogradov, V. A. Ferapontov, Sergei G. Zlotin, O. V. Turova, Nikolai S. Ikonnikov, Ilya V. Kuchurov
Publikováno v:
Mendeleev Communications. 22:184-186
Asymmetric hydrogenation of ethyl 4-chloro-3-oxobutyrate and dimethyl acetylsuccinate in high pressure CO 2 using [RuCl 2 (C 6 H 6 )] 2 –( R )-BINAP as the catalyst provides high ee values for the products.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::460fd52e19268aaa175c13929834995c
https://doi.org/10.1016/j.mencom.2012.06.003
https://doi.org/10.1016/j.mencom.2012.06.003
Autor:
M. G. Vinogradov, V. A. Pavlov, G. L. Heise, E. V. Starodubtseva, V. A. Ferapontov, O. R. Malyshev
Publikováno v:
Russian Chemical Bulletin. 49:728-731
The catalytic activity and the enantioselectivity manifested by cationic chiral binaphthylbisphosphine ruthenium complexes in asymmetric hydrogenation of β-keto esters were studied. The effects of the nature of the solvent, the reaction temperature,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::69c0cff42e0128f7b8b03acae2ae25e0
https://doi.org/10.1007/bf02495491
https://doi.org/10.1007/bf02495491
Autor:
G. V. Chel'tsova, L. S. Gorshkova, I. V. Razmanov, V. A. Ferapontov, O. R. Malyshev, M. G. Vinogradov, O. V. Mikhalev, G. L. Heise, V. A. Pavlov
Publikováno v:
Russian Chemical Bulletin. 49:460-465
New stereoselective reducing reagents were preparedin situ by modification of NaAlH4 with various chiral diols. The efficiency of 1,4- and 1,3-diols as chiral auxiliaries in the reactions of alkyl aryl ketones with modified NaAlH4 was considerably hi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9bc16fb8aee01bb9a3d91d0a9d344a8c
https://doi.org/10.1007/bf02494775
https://doi.org/10.1007/bf02494775