Unexpected dimerization of 5,7-dimethyl-2-trifluoromethyl-8-azachromone induced by hydrogen sulfide / Barabanov M. A.,Sosnovskikh V. Ya.,Moshkin V. S.,Kodess M. I. // RUSSIAN CHEMICAL BULLETIN. - 2010. - V. 59, l. 11. - P. 2094-2097.

ISSN/EISSN:

1066-5285 / нет данных

Type:

Article

Abstract:

Depending on the reaction conditions, the reaction of 5,7-dimethyl-2-trifluoromethyl-8-azachromone with hydrogen sulfide afforded cyclic and linear dimers with the S-S bond. The regio- and stereochemistry of the reaction products were determined by (1)H and (13)C NMR spectroscopy.

Author keywords:

5,7-dimethyl-2-trifluoromethyl-8-azachromone; hydrogen sulfide; dimerization; 1,2-dithiolane; disulfides; NMR spectroscopy REDOX REACTION; 8-AZA-5,7-DIMETHYL-2-TRIFLUOROMETHYLCHROMONE; REACTIVITY

DOI:

10.1007/s11172-010-0360-4

Web of Science ID:

ISI:000289006200011

Соавторы в МНС:

Другие поля

Поле	Значение
Month	NOV
Publisher	SPRINGER
Address	233 SPRING ST, NEW YORK, NY 10013 USA
Language	English
Keywords-Plus	REDOX REACTION; 8-AZA-5,7-DIMETHYL-2-TRIFLUOROMETHYLCHROMONE; REACTIVITY
Research-Areas	Chemistry
Web-of-Science-Categories	Chemistry, Multidisciplinary
Author-Email	Vyacheslav.Sosnovskikh@usu.ru
ResearcherID-Numbers	Moshkin, Vladimir/E-6623-2017
Number-of-Cited-References	17
Usage-Count-Last-180-days	1
Usage-Count-Since-2013	2
Journal-ISO	Russ. Chem. Bull.
Doc-Delivery-Number	743GR