Reactions of 3-nitro-2-trihalomethyl-2H-chromenes with indole, N-methylindole, and N-methylpyrrole. Stereoselective synthesis of 4-azolyl-3-nitro-2-trihalomethylchromanes / Korotaev V. Yu.,Sosnovskikh V. Ya.,Kutyashev I. B. // RUSSIAN CHEMICAL BULLETIN. - 2007. - V. 56, l. 10. - P. 2054-2059.

ISSN/EISSN:

1066-5285 / нет данных

Type:

Article

Abstract:

Heating of 3-nitro-2-trifluoromethyl-and 3-nitro-2-trichloromethyl-2H-chromenes with indole, N-methylindole, and N-methylpyrrole under solvent-free conditions led with high stereoselectivity and in good yields to cis-trans-3-nitro-2-trifluoromethyl-or trans-cis-3-nitro-2-trichloromethylchromanes substituted by the indol-3-yl (pyrrol-2-yl) fragment in position 4.

Author keywords:

chromenes; chromanes; indoles; N-methylpyrrole; stereoselectivity; diastereomers; NMR spectroscopy POTASSIUM CHANNEL ACTIVATORS; ANTIHYPERTENSIVE ACTIVITY; C-NUCLEOPHILES; S-NUCLEOPHILES; NITROALKENES

DOI:

10.1007/s11172-007-0321-8

Web of Science ID:

ISI:000254206300022

Соавторы в МНС:

Другие поля

Поле	Значение
Month	OCT
Publisher	SPRINGER
Address	233 SPRING STREET, NEW YORK, NY 10013 USA
Language	English
Keywords-Plus	POTASSIUM CHANNEL ACTIVATORS; ANTIHYPERTENSIVE ACTIVITY; C-NUCLEOPHILES; S-NUCLEOPHILES; NITROALKENES
Research-Areas	Chemistry
Web-of-Science-Categories	Chemistry, Multidisciplinary
Author-Email	Vyacheslav.Sosnovskikh@usu.ru
ResearcherID-Numbers	Korotaev, Vladislav/L-2692-2016
ORCID-Numbers	Korotaev, Vladislav/0000-0002-7492-5116
Number-of-Cited-References	19
Usage-Count-Last-180-days	1
Usage-Count-Since-2013	3
Journal-ISO	Russ. Chem. Bull.
Doc-Delivery-Number	277IQ