Synthesis of polyfunctionalized benzophenones via the reaction of 3-formylchromones with tertiary push-pull enamines / Barkov Alexey Yu.,Korotaev Vladislav Yu.,Kutyashev Igor B.,Sosnovskikh Vyacheslav Ya. // TETRAHEDRON. - 2016. - V. 72, l. 16. - P. 2026-2033.

ISSN/EISSN:

0040-4020 / нет данных

Type:

Article

Abstract:

Uncatalyzed nucleophilic reaction of 3-formylchromones with tertiary push pull enamines in refluxing acetonitrile gave polyfunctionalized benzophenone derivatives as a result of a {[}3-1-3] annulation in moderate to good yields. (C) 2016 Elsevier Ltd. All rights reserved.

Author keywords:

3-Formylchromones; Enaminones; Benzophenones HETEROCYCLIC-SYSTEMS; COMBINATORIAL SYNTHESIS; ENOL ETHERS; 4-OXO-4H-1-BENZOPYRAN-3-CARBOXALDEHYDE; DERIVATIVES; CHEMISTRY; ROUTE; BENZOPYRANS

DOI:

10.1016/j.tet.2016.03.005

Web of Science ID:

ISI:000374198700018

Соавторы в МНС:

Другие поля

Поле	Значение
Month	APR 21
Publisher	PERGAMON-ELSEVIER SCIENCE LTD
Address	THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND
Language	English
Keywords-Plus	HETEROCYCLIC-SYSTEMS; COMBINATORIAL SYNTHESIS; ENOL ETHERS; 4-OXO-4H-1-BENZOPYRAN-3-CARBOXALDEHYDE; DERIVATIVES; CHEMISTRY; ROUTE; BENZOPYRANS
Research-Areas	Chemistry
Web-of-Science-Categories	Chemistry, Organic
Author-Email	vy.sosnovskikh@urfu.ru
ResearcherID-Numbers	Korotaev, Vladislav/L-2692-2016
ORCID-Numbers	Korotaev, Vladislav/0000-0002-7492-5116
Funding-Acknowledgement	Government of the Russian Federation {[}02.A03.21.0006]
Funding-Text	This work was financially supported by the Act 211 Government of the Russian Federation, agreement No 02.A03.21.0006, and performed within the State Task from the Ministry of Education and Science of Russian Federation.
Number-of-Cited-References	38
Usage-Count-Last-180-days	1
Usage-Count-Since-2013	16
Journal-ISO	Tetrahedron
Doc-Delivery-Number	DJ4SQ