Synthesis of trans-2-(indol-3-yl)-3-nitrothiochroman-4-ones from 3-nitrothiochromone and indoles / Barabanov M. A.,Sevenard D. V.,Sosnovskikh V. Ya. // RUSSIAN CHEMICAL BULLETIN. - 2012. - V. 61, l. 11. - P. 2183-2185.

ISSN/EISSN:

1066-5285 / нет данных

Type:

Article

Abstract:

1,4-Nucleophilic addition reactions of 3-nitrothiochromone with indoles gave a number of novel trans-2-(indol-3-yl)-3-nitrothiochroman-4-ones in 36-89\% yields. During the reactions, the thiopyrone ring underwent no opening.

Author keywords:

3-nitrothiochromone; indoles; the Michael addition; 2-(indol-3-yl)-3-nitrothiochroman-4-ones N-METHYLPYRROLE; UNCATALYZED ADDITION; E-2-HYDROXY-3-(1-METHYLPYRROL-2-YLMETHYLENE)CHROMAN-4-ONES; (CHROMON-3-YL)BIS(INDOL-3-YL)METHANES; 3-(POLYFLUOROACYL)CHROMONES; CYCLOCONDENSATION; 3-FORMYLCHROMONES; 3-NITROCHROMONE; DERIVATIVES; CHEMISTRY

DOI:

10.1007/s11172-012-0308-y

Web of Science ID:

ISI:000322877300025

Соавторы в МНС:

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Другие поля

Поле	Значение
Month	NOV
Publisher	SPRINGER
Address	233 SPRING ST, NEW YORK, NY 10013 USA
Language	English
Keywords-Plus	N-METHYLPYRROLE; UNCATALYZED ADDITION; E-2-HYDROXY-3-(1-METHYLPYRROL-2-YLMETHYLENE)CHROMAN-4-ONES; (CHROMON-3-YL)BIS(INDOL-3-YL)METHANES; 3-(POLYFLUOROACYL)CHROMONES; CYCLOCONDENSATION; 3-FORMYLCHROMONES; 3-NITROCHROMONE; DERIVATIVES; CHEMISTRY
Research-Areas	Chemistry
Web-of-Science-Categories	Chemistry, Multidisciplinary
Author-Email	Vyacheslav.Sosnovskikh@usu.ru
Number-of-Cited-References	24
Usage-Count-Last-180-days	1
Usage-Count-Since-2013	3
Journal-ISO	Russ. Chem. Bull.
Doc-Delivery-Number	197UP