1-ALKYL-1,2,4-TRIAZINIUM YLIDES AS 1,3-DIPOLES IN A CYCLOADDITION REACTION WITH DIETHYL ACETYLENEDICARBOXYLATE / CHUPAKHIN ON,RUDAKOV BV,ALEXEEV SG,SHORSHNEV SV,CHARUSHIN VN // MENDELEEV COMMUNICATIONS. - 1992. - V. , l. 3. - P. 85-86.

ISSN/EISSN:

0959-9436 / нет данных

Type:

Article

Abstract:

Deprotonation of 1-alkyl-5-phenyl-1,2,4-triazinium salts by triethylamine results in the formation of azomethyne ylides which undergo a 1,3-dipolar cycloaddition reaction with diethyl acetylenedicarboxylate to yield pyrrolo{[}2,1-f]1,2,4-triazines.

Author keywords:

нет данных

DOI:

нет данных

Web of Science ID:

ISI:A1992JG80600004

Соавторы в МНС:

Другие поля

Поле	Значение
Month	AUG
Publisher	ROYAL SOC CHEMISTRY
Address	THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON ROAD, CAMBRIDGE, CAMBS, ENGLAND CB4 4WF
Language	English
Research-Areas	Chemistry
Web-of-Science-Categories	Chemistry, Multidisciplinary
Number-of-Cited-References	12
Journal-ISO	Mendeleev Commun.
Doc-Delivery-Number	JG806