Reaction of 4,5-dimethoxy-1,2-dehydrobenzene with 3-(Pyridin-2-yl)-1,2,4-triazines / Kopchuk D. S.,Nikonov I. L.,Zyryanov G. V.,Kovalev I. S.,Taniya O. S.,Rusinov V. L.,Chupakhin O. N. // RUSSIAN JOURNAL OF ORGANIC CHEMISTRY. - 2015. - V. 51, l. 8. - P. 1170-1173.

ISSN/EISSN:

1070-4280 / 1608-3393

Type:

Article

Abstract:

Reaction of 3-(pyridin-2-yl)-1,2,4-triazines with aryne intermediate, 4,5-dimethoxy-1,2-dehydrobenzene generated in situ, was investigated. As a result of the interaction products of the 1,2,4-triazine transformation are produced: 2,3-dimethoxy-10-(1H-1,2,3-triazol-1-yl)-pyrido{[}1,2-a]indoles, and also the products of Diels-Alder aza-reaction, 6,7-dimethoxy-1-(pyridin-2-yl)isoquinolines.

Author keywords:

ISOQUINOLINE ALKALOIDS; ARYNE; HETEROCYCLES; LIGANDS; ANALOGS

DOI:

10.1134/S1070428015080175

Web of Science ID:

ISI:000361905700017

Соавторы в МНС:

Другие поля

Поле	Значение
Month	AUG
Publisher	MAIK NAUKA/INTERPERIODICA/SPRINGER
Address	233 SPRING ST, NEW YORK, NY 10013-1578 USA
Language	English
EISSN	1608-3393
Keywords-Plus	ISOQUINOLINE ALKALOIDS; ARYNE; HETEROCYCLES; LIGANDS; ANALOGS
Research-Areas	Chemistry
Web-of-Science-Categories	Chemistry, Organic
Author-Email	gvzyryanov@gmail.com
Funding-Acknowledgement	President's Grants Council {[}MK-3079.2015.3]; Russian Government {[}02.A03.21.0006]; Ural Branch of the Russian Academy of Sciences {[}13-3-028 SG]
Funding-Text	This research was carried out with the financial support of the President's Grants Council (grant MK-3079.2015.3), program 211 of the Russian Government (contract no. 02.A03.21.0006), and the program of targeted fundamental research of the Ural Branch of the Russian Academy of Sciences (no. 13-3-028 SG).
Number-of-Cited-References	30
Usage-Count-Last-180-days	3
Usage-Count-Since-2013	13
Journal-ISO	Russ. J. Organ. Chem.
Doc-Delivery-Number	CS2MR