Please use this identifier to cite or link to this item: http://elar.urfu.ru/handle/10995/51160
Title: Self condensation of enamines mediated by acetylation. A novel approach to 1-(azol-5-yl)-(1E,3Z)-butadiene-4-N,N-dimethylamines
Authors: Shafran, Yuri
Rozin, Yuri
Beryozkina, Tetyana
Zhidovinov, S. S.
Eltsov, Oleg
Subbotina, Julia
Leban, Johann
Novikova, Rashida
Bakulev, Vasiliy
Issue Date: 2012
Publisher: Springer Berlin Heidelberg
Citation: Self condensation of enamines mediated by acetylation. A novel approach to 1-(azol-5-yl)-(1E,3Z)-butadiene-4-N,N-dimethylamines / Yuri Shafran, Yuri Rozin, Tetyana Beryozkina, S. S. Zhidovinov, Oleg Eltsov, Julia Subbotina, Johann Leban, Rashida Novikova, Vasiliy Bakulev // Organic and Biomolecular Chemistry. — 2012. — Vol. 10. — № 30. — P. 5795-5798.
Abstract: Novel self-condensation of 3-(azol-5-yl)-1,1-dimethylenamines has been found to form new C-C bonds leading to 2,4-(1,2,3-triazole-1,2,3-thiadiazole-3- phenylisothiazole)-(1E,3Z)-5-yl-butadiene-1-amines. The discovered reaction represents a new example of C-H functionalization in unsaturated systems and can serve an efficient synthetic approach to rational design of new 2,4-(diazole-5-yl)-dieneamines. © 2012 The Royal Society of Chemistry.
URI: http://elar.urfu.ru/handle/10995/51160
SCOPUS ID: 84863915113
WOS ID: 000306276800020
PURE ID: 1077260
ISSN: 1477-0520
1477-0539
DOI: 10.1039/c2ob25331c
Appears in Collections:Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.