Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Fatima A. Tsiunchik"'
Autor:
Maxim G. Uchuskin, Alexander V. Butin, Olga N. Kostyukova, Fatima A. Tsiunchik, Igor V. Trushkov
Publikováno v:
Synthesis. 2011:2629-2638
A new approach to highly functionalized quinolines is proposed.This approach is based on the electrophilic recyclization of 2-[2-(acylamino)benzyl]furansunder the Bischler-Napieralski reaction conditions.
Autor:
Arkady S. Pilipenko, Alexander V. Butin, Igor V. Trushkov, Maxim G. Uchuskin, Fatima A. Tsiunchik, Dmitry A. Cheshkov
Publikováno v:
European Journal of Organic Chemistry. 2010:920-926
A new simple approach to 3-(2-acylvinyl)-2-(hetero)aryl-indoles has been developed. The method is based on the acid-catalysed interaction of 2-(2-aminophenyl)furans with (hetero)aromatic aldehydes. The reactions proceed under very mild conditions and
Autor:
Alexander V. Butin, Vladimir T. Abaev, Fatima A. Tsiunchik, Dmitry A. Cheshkov, Andrey Gutnov
Publikováno v:
Synthesis. 2009:2616-2626
A new rearrangement of 1-(diarylmethyl)-2-isothiocy-anatobenzenes into 2,4-diaryl-4H-3,1-benzothiazine derivatives is described. Treatment of the starting compounds with aluminum trichloride under Friedel-Crafts conditions leads to migration of an ar
Publikováno v:
Arkivoc. 2009:79-87
Treatment of 1-(2-isothiocyanoaryl)-2-(2-furyl)ethane with anhydrous aluminum chloride under Friedel-Crafts conditions yielded a pyrrolo[1,2-a]quinoline derivative via electrophilic attack of the activated isothiocyano group onto the furan ring. The
Autor:
Alexander V. Butin, Fatima A. Tsiunchik, Igor V. Trushkov, Maxim G. Uchuskin, Sergey K. Smirnov
Publikováno v:
Synthesis. 2008:2943-2952
The recyclization of (2-aminophenyl)bis(5-tert-butyl-2-furyl)methanes under acidic conditions was studied. It was found that the extent of reaction of these substrates depends on the substituent at the nitrogen atom of the aniline moiety. N-Tosyl der
Publikováno v:
Synlett. 2008:1145-1148
A simple and effective method has been elaborated for the synthesis of thieno[2,3- B]indole ring system. It is based on the electrophilic recyclization of 2-alkyl-5-(2-isothiocyanoaryl)furans in the presence of anhydrous AlCl 3 .
Publikováno v:
Journal of Heterocyclic Chemistry. 45:475-481
A new simple synthetic approach to 2,4-difuryl-4H-3,1-benzothiazines from 2-isothiocyanoaryldifuryl-methanes in the presence of acidic catalyst is described. This rearrangement is a new example of furan ring migration reaction resulting from intramol
Publikováno v:
Tetrahedron Letters. 47:4029-4032
A new synthetic approach to 2,4-diaryl-4 H -3,1-benzothiazines is described based on the rearrangement of 2-isothiocyano triarylmethanes in the presence of AlCl 3 . An aryl ring is found to migrate to the carbon atom of an isothiocyano group followed
Publikováno v:
Chemistry of Heterocyclic Compounds. 47:644-646
Publikováno v:
Chemistry of Heterocyclic Compounds. 46:1539-1541