Synthesis of 2H-azolo{[}1,5-a]{[}1,2,3]triazolo{[}4,5-e]pyrimidines / Gorbunov Evgeny B.,Rusinov Gennady L.,Ulomskii Evgeny N.,Isenov Maksim L.,Charushin Valery N. // CHEMISTRY OF HETEROCYCLIC COMPOUNDS. - 2015. - V. 51, l. 5. - P. 491-495.

ISSN/EISSN:

0009-3122 / 1573-8353

Type:

Article

Abstract:

6-Nitroazolo{[}1,5-a]pyrimidines were used as dipolarophiles in a reaction with sodium azide providing previously unknown 2De-azolo{[}1,5-a]-{[}1,2,3]triazolo{[}4,5-e]pyrimidines.

Author keywords:

azapurines; 6-nitroazolo{[}1,5-alpha]pyrimidines; catalytic hydrogenation; 1,3-dipolar cycloaddition A(1) ADENOSINE RECEPTORS; CARBOCYCLIC NUCLEOSIDES; INHIBITORS; ANALOGS; DESIGN; IDENTIFICATION; ANTAGONISTS; DEAMINASE

DOI:

10.1007/s10593-015-1725-2

Web of Science ID:

ISI:000358138200012

Соавторы в МНС:

Другие поля

Поле	Значение
Month	MAY
Publisher	SPRINGER
Address	233 SPRING ST, NEW YORK, NY 10013 USA
Language	English
EISSN	1573-8353
Keywords-Plus	A(1) ADENOSINE RECEPTORS; CARBOCYCLIC NUCLEOSIDES; INHIBITORS; ANALOGS; DESIGN; IDENTIFICATION; ANTAGONISTS; DEAMINASE
Research-Areas	Chemistry
Web-of-Science-Categories	Chemistry, Organic
Author-Email	nitro@ios.uran.ru
Funding-Acknowledgement	Russian Foundation for Basic Research {[}14-03-31385\_mol a]; Russian Science Foundation {[}14-13-01301]
Funding-Text	This work was performed with financial support from the Russian Foundation for Basic Research (project 14-03-31385\_mol a) and the Russian Science Foundation (project 14-13-01301).
Number-of-Cited-References	27
Usage-Count-Last-180-days	1
Usage-Count-Since-2013	5
Journal-ISO	Chem. Heterocycl. Compds.
Doc-Delivery-Number	CN0XN