Zobrazeno 1 - 10
of 58
pro vyhledávání: '"Alexey B. Zaitsev"'
Autor:
Elena Yu. Schmidt, Al’bina I. Mikhaleva, Alexander M. Vasil’tsov, Alexey B. Zaitsev, Nadezhda V. Zorina
Publikováno v:
ARKIVOC, Vol 2005, Iss 7, Pp 11-17 (2005)
Externí odkaz:
https://doaj.org/article/3988756badc54964b7744b5371ba8977
Autor:
Elena Yu. Schmidt, Alexander M. Vasil’tsov, Al’bina I. Mikhaleva, Alexey B. Zaitsev, Andrey V. Afonin, Dar’ya-Syren D. Toryashinova, Ludmila V. Klyba, Jan-Dirk Arndt, Jochem Henkelmann
Publikováno v:
ARKIVOC, Vol 2003, Iss 13, Pp 35-44 (2003)
Externí odkaz:
https://doaj.org/article/eee56d6b633c428ea49cb19e07711a45
Publikováno v:
Chemistry - A European Journal. 15:6468-6477
Green and fast: Allylation of aromatic and aliphatic thiols, by using allyl alcohols as substrates, requires only minutes at ambient temperature with a Ru catalyst (see scheme). Quantitative conversion is normal and the catalyst possesses high functi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9eceaab2c72baf88edf75aa9870c3fb
https://doi.org/10.1002/chem.200900192
https://doi.org/10.1002/chem.200900192
Publikováno v:
Organometallics. 28:3437-3448
The Ru-catalyzed allylation of differing indole compounds using ArCH(OH)CH═CH2 (Ar = Ph, 2-CH3C6H4, 2-CH3OC6H4 2-ClC6H4, and 1-naphthyl) is relatively fast (usually
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::21c9250e332466e62e9de1eaf723bbe2
https://doi.org/10.1021/om900168y
https://doi.org/10.1021/om900168y
Publikováno v:
Organometallics. 27:3796-3805
The dicationic Ru(IV) salt [Ru(Cp*)(η3-C3H5)(CH3CN)2](PF6)2 is shown to be an excellent and rapid catalyst for the C-allylation of indole compounds using allyl alcohols as substrates. Selective, one-pot N,C-double allylation is also possible. Prelim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::453f964893c0059665153fe25c702a3d
https://doi.org/10.1021/om800295z
https://doi.org/10.1021/om800295z
Publikováno v:
Advanced Synthesis & Catalysis. 349:2556-2562
Rhodium-Catalyzed Asymmetric Transfer Hydrogenation of Aryl Alkyl Ketones Employing Ligands Derived from Amino Acids
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f2f3c66a0fcd8e2221005df8eea43e24
https://doi.org/10.1002/adsc.200700345
https://doi.org/10.1002/adsc.200700345
Publikováno v:
Synlett. 2007:2541-2544
Aryl alkyl ketones are efficiently and selectively reduced (up to 97% ee) under transfer-hydrogenation conditions in 2-propanol using rhodium catalysts based on readily available amino acid derived hydroxamic acid ligands.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b439ea7d6e216112d155d1bcdacd8c47
https://doi.org/10.1055/s-2007-986653
https://doi.org/10.1055/s-2007-986653
Autor:
Andrey V. Ivanov, Boris A. Trofimov, Elena Yu. Schmidt, Al'bina I. Mikhaleva, Cristina Pozo-Gonzalo, Nadezhda V. Zorina, Javier Rodriguez, Alexey B. Zaitsev, Alexander M. Vasil'tsov, José A. Pomposo
Publikováno v:
Synthetic Metals. 157:60-65
A series of 2,2'-dipyrrole monomers separated by aza-spacers (N,N'-bis-(1H-pyrrol-2-ylmethylene)-benzene-1,4-diamine; N-4,N-4'-bis(1H-pyrrol-2-ylmethylene)-biphenyl-4,4'-diamine; N,N'-bis-[1-(1H-py ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::39f5812eca14b9390022d956ee27c54e
https://doi.org/10.1016/j.synthmet.2006.12.002
https://doi.org/10.1016/j.synthmet.2006.12.002
Publikováno v:
Russian Chemical Reviews. 75:797-823
Data on the chemical properties of oximes and their derivatives widely used in the synthesis of different nitrogen-containing acyclic and heterocyclic compounds are systematised and analysed. The polyfunctional nature of oximes is emphasised and thei
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d7ccdd09a2568dc0f1186608d369ec6
https://doi.org/10.1070/rc2006v075n09abeh003594
https://doi.org/10.1070/rc2006v075n09abeh003594
Autor:
Al'bina I. Mikhaleva, Konstantin B. Petrushenko, A. V. Afonin, Natalia S. Smolyanina, Elena Yu. Senotrusova, Alexander F. Schmidt, Alexander M. Vasil'tsov, Elena Yu. Schmidt, Igor A. Ushakov, Marina V. Markova, Alexey B. Zaitsev, V. V. Smirnov, Boris A. Trofimov, Olga N. Kazheva, Ludmila V. Morozova, Oleg A. Dyachenko
Publikováno v:
European Journal of Organic Chemistry. 2006:4021-4033
New reactive dyes, 2-arylazo-1-vinylpyrroles, have been synthesized in 52–94 % yield by a modified azo coupling of readily accessible 1-vinylpyrroles with arenediazonium hydrocarbonates in aqueous ethanol (≈3:1) at 0 °C. The λmax values for the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::93fca656d11005d374bda25241c4ad71
https://doi.org/10.1002/ejoc.200600357
https://doi.org/10.1002/ejoc.200600357