Synthesis of 1,2,3-triazolo{[}1,5-a]pyridin-8-ium-3-olates / Khazhieva Inna S.,Demkin Pavel M.,Nein Julia I.,Glukhareva Tatiana V.,Morzherin Yuri Yu. // CHEMISTRY OF HETEROCYCLIC COMPOUNDS. - 2015. - V. 51, l. 2. - P. 199-202.

ISSN/EISSN:

0009-3122 / 1573-8353

Type:

Article

Abstract:

Alkylation of sodium 4-acetyl-1-phenyl-1,2,3-triazol-5-olate with alpha-bromoacetophenones was shown to occur at position 3 of the heterocycle, with the formation of 1,2,3-triazol-3-ium-5-olates. Intramolecular crotonic condensation of the latter led to the formation of 1,2,3-triazolo{[}1,5-D degrees]pyridin-8-ium-3-olates.

Author keywords:

azoles; fused heterocycles; mesoionic heterocycles; pyridines; 1,2,3-triazoles; 1,2,3-triazol-3-ium-5-olates; alkylation; crotonic condensation; heterocyclization

DOI:

10.1007/s10593-015-1681-x

Web of Science ID:

ISI:000353057900014

Соавторы в МНС:

Другие поля

Поле	Значение
Month	FEB
Publisher	SPRINGER
Address	233 SPRING ST, NEW YORK, NY 10013 USA
Language	English
EISSN	1573-8353
Research-Areas	Chemistry
Web-of-Science-Categories	Chemistry, Organic
Author-Email	yu.yu.morzherin@urfu.ru
ResearcherID-Numbers	Morzherin, Yury/M-7420-2013 Glukhareva, Tatiana/A-4610-2016 Nein, Juliya/P-4340-2016
ORCID-Numbers	Morzherin, Yury/0000-0002-1333-6676 Glukhareva, Tatiana/0000-0002-5231-9879 Nein, Juliya/0000-0003-0569-5713
Funding-Acknowledgement	Ministry of Education and Science of the Russian Federation {[}4.560.2014-K]; Russian Foundation for Basic Research {[}13-03-00137]
Funding-Text	The results were obtained within the framework of the State Assignment for sscientific activity No. 4.560.2014-K from the the Ministry of Education and Science of the Russian Federation and with support from the Russian Foundation for Basic Research (grant 13-03-00137).
Number-of-Cited-References	14
Usage-Count-Last-180-days	1
Usage-Count-Since-2013	11
Journal-ISO	Chem. Heterocycl. Compds.
Doc-Delivery-Number	CG1TS