Reactions of 5-dialkylamino-1,2,3-thiadiazole-4-carbaldehydes with amines as a method for the synthesis of 1,2,3-triazole-4-carbothioamides / Glukkarev TV,Morzherin YY,Dyudya LV,Malysheva KV,Tkachev AV,Padva A,Bakulea VA // RUSSIAN CHEMICAL BULLETIN. - 2004. - V. 53, l. 6. - P. 1311-1317.

ISSN/EISSN:

1066-5285 / нет данных

Type:

Article

Abstract:

A method for the synthesis of previously inaccessible 5-dialkylamino-substituted 1,2,3-thiadiazole-4-carbaldehydes was developed. Ring transformation in these compounds induced by primary aliphatic and aromatic amines, hydroxylamines, and N-substituted hydrazines resulted in the synthesis of a broad range of 1,2,3-triazole-4-carbothioamide.

Author keywords:

1,2,3-triazole; 1,2,3-thiadiazole; thioamides; cornfort rearrangement; nucleophilic substitution; reduction; oxidation REARRANGEMENT; DERIVATIVES; 1,2,3-THIADIAZOLES; THIOAMIDES; SYSTEM

DOI:

10.1023/B:RUCB.0000042292.1911

Web of Science ID:

ISI:000224147800027

Соавторы в МНС:

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Другие поля

Поле	Значение
Month	JUN
Publisher	CONSULTANTS BUREAU
Address	233 SPRING ST, NEW YORK, NY 10013 USA
Language	English
Keywords-Plus	REARRANGEMENT; DERIVATIVES; 1,2,3-THIADIAZOLES; THIOAMIDES; SYSTEM
Research-Areas	Chemistry
Web-of-Science-Categories	Chemistry, Multidisciplinary
Author-Email	chemap@emory.edu morjerine@htf.ustu.ru atkachev@nioch.nsc.ru
ResearcherID-Numbers	Morzherin, Yury/M-7420-2013
ORCID-Numbers	Morzherin, Yury/0000-0002-1333-6676
Number-of-Cited-References	20
Usage-Count-Since-2013	1
Journal-ISO	Russ. Chem. Bull.
Doc-Delivery-Number	857VR