Perfluoro(1,2-epoxycyclohexane) in the synthesis of fluorinated heterocycles / Filyakova T. I.,Zapevalov A. Ya.,Kodess M. I.,Slepukhin P. A.,Saloutin V. I. // RUSSIAN JOURNAL OF ORGANIC CHEMISTRY. - 2014. - V. 50, l. 6. - P. 854-857.

ISSN/EISSN:

1070-4280 / 1608-3393

Type:

Article

Abstract:

Perfluoro(1,2-epoxycyclohexane) readily reacts with bifunctional nucleophiles (urea, thiourea, and benzene-1,2-diamine) via opening of the oxirane ring and subsequent heterocyclization to give fluorinated benzimidazole, 1,3-benzothiazole, and phenazine derivatives, respectively.

Author keywords:

EPOXIDES; THIOUREA

DOI:

10.1134/S1070428014060177

Web of Science ID:

ISI:000338997900017

Соавторы в МНС:

Другие поля

Поле	Значение
Month	JUN
Publisher	MAIK NAUKA/INTERPERIODICA/SPRINGER
Address	233 SPRING ST, NEW YORK, NY 10013-1578 USA
Language	English
EISSN	1608-3393
Keywords-Plus	EPOXIDES; THIOUREA
Research-Areas	Chemistry
Web-of-Science-Categories	Chemistry, Organic
Author-Email	fc403@ios.uran.ru
Funding-Acknowledgement	Ural Branch, Russian Academy of Sciences {[}12-P-3-1030]; Council for Grants at the President of the Russian Federation {[}NSh-3656.2014.3]
Funding-Text	This study was performed under financial support by the Ural Branch, Russian Academy of Sciences (project no. 12-P-3-1030) and by the Council for Grants at the President of the Russian Federation (project no. NSh-3656.2014.3).
Number-of-Cited-References	17
Usage-Count-Last-180-days	1
Usage-Count-Since-2013	7
Journal-ISO	Russ. J. Organ. Chem.
Doc-Delivery-Number	AL3AS