Solvent-free reaction of 3-aryl-6-(3-nitrophenyl)-1,2,4-triazines with 4-(cyclohex-1-en-1-yl)morpholine / Kopchuk D. S.,Khasanov A. F.,Krinochkin A. P.,Kovalev I. S.,Zyryanov G. V.,Rusinov V. L.,Chupakhin O. N. // RUSSIAN JOURNAL OF ORGANIC CHEMISTRY. - 2016. - V. 52, l. 7. - P. 1036-1038.

ISSN/EISSN:

1070-4280 / 1608-3393

Type:

Article

Abstract:

The aza-Diels-Alder reaction of 3-aryl-6-(3-nitrophenyl)-1,2,4-triazines with 4-(cyclohex-1-en-1-yl)morpholine as dienophile was accompanied by reduction of the nitro group to amino. In the reaction of 3-(4-methoxyphenyl)-6-(3-nitrophenyl)-1,2,4-triazine with 4-(cyclohex-1-en-1-yl)morpholine, 3-{[}3-(4-methoxyphenyl)-1,2,4-triazin-6-yl)aniline was formed together with the cycloaddition product.

Author keywords:

DIELS-ALDER REACTION; SUBSTITUTED PYRIDINES; 1,2,4-TRIAZINES; COMPLEXES

DOI:

10.1134/S1070428016070204

Web of Science ID:

ISI:000382093600020

Соавторы в МНС:

Другие поля

Поле	Значение
Month	JUL
Publisher	MAIK NAUKA/INTERPERIODICA/SPRINGER
Address	233 SPRING ST, NEW YORK, NY 10013-1578 USA
Language	English
EISSN	1608-3393
Keywords-Plus	DIELS-ALDER REACTION; SUBSTITUTED PYRIDINES; 1,2,4-TRIAZINES; COMPLEXES
Research-Areas	Chemistry
Web-of-Science-Categories	Chemistry, Organic
Author-Email	gvzyryanov@gmail.com
Funding-Acknowledgement	Russian Science Foundation {[}16-43-02 020]
Funding-Text	This study was performed under financial support by the Russian Science Foundation (project no. 16-43-02 020).
Number-of-Cited-References	12
Usage-Count-Last-180-days	2
Usage-Count-Since-2013	4
Journal-ISO	Russ. J. Organ. Chem.
Doc-Delivery-Number	DU3EM