Self-condensation of 3-cyanothiochromone upon the action of benzyl- and phenethylamine / Sosnovskikh V. Ya.,Sevenard D. V.,Moshkin V. S.,El'tsov O. S. // RUSSIAN CHEMICAL BULLETIN. - 2010. - V. 59, l. 11. - P. 2155-2158.

ISSN/EISSN:

1066-5285 / нет данных

Type:

Article

Abstract:

Reflux of 3-cyanothiochromone with benzylamine in toluene afforded 17-benzyl-6,7,14,15-tetrahydro-7,15-epiminobis(8H,16H-dithiochromeno){[} 2,3-b:2',3'-f]{[}1,5]diazocine-6,14-dione, the self-condensation product of 2-amino-3-(benzyliminomethyl)thiochromone. Similar reaction with phenethylamine leads to 2-(thiochromon-3-yl)-5H-thiochromeno{[}2,3-d]-pyrimidin-5-one. Mechanism of formation of the dimeric products was considered.

Author keywords:

3-cyanothiochromone; benzylamine; phenethylamines; self-condensation; 17-benzyl-6,7,14,15-tetrahydro-7,15-epiminobis(8H,16H-dithiochromeno){[} 2,3-b:2 `,3 `-f]{[}1,5]diazocine-6,14-dione; 2-(4-oxo-4H- CHROMONES

DOI:

10.1007/s11172-010-0373-z

Web of Science ID:

ISI:000289006200024

Соавторы в МНС:

Другие поля

Поле	Значение
Month	NOV
Publisher	SPRINGER
Address	233 SPRING ST, NEW YORK, NY 10013 USA
Language	English
Keywords-Plus	CHROMONES
Research-Areas	Chemistry
Web-of-Science-Categories	Chemistry, Multidisciplinary
Author-Email	vyacheslav.sosnovskikh@usu.ru
ResearcherID-Numbers	Moshkin, Vladimir/E-6623-2017
Number-of-Cited-References	10
Usage-Count-Last-180-days	1
Usage-Count-Since-2013	2
Journal-ISO	Russ. Chem. Bull.
Doc-Delivery-Number	743GR