Unusual ring-chain tautomerism in bicyclo{[}4.2.0]octane derivatives / Korotaev Vladislav Yu.,Barkov Alexey Yu.,Slepukhin Pavel A.,Kodess Mikhail I.,Sosnovskikh Vyacheslav Ya. // TETRAHEDRON LETTERS. - 2011. - V. 52, l. 23. - P. 3029-3032.

ISSN/EISSN:

0040-4039 / нет данных

Type:

Article

Abstract:

A new type of ring-chain tautomerism, which consists of the reversible conversion of bicyclo{[}4.2.0)octane derivatives into trisubstituted enamines was found and studied by (1)H NMR spectroscopy. The starting materials were prepared by the stereoselective reaction of (E)-3,3,3-trichloro-1-nitropropene with cyclohexanone enamines. (C) 2011 Elsevier Ltd. All rights reserved.

Author keywords:

Cyclobutanes; Nitroalkenes; Enamines; Ring-chain tautomerism; (1)H NMR spectroscopy CYCLIC NITRONIC ESTERS; CYCLOADDITION REACTIONS; CYCLOHEXANONE ENAMINES; N-OXIDE; NITROOLEFINS; OLEFINS; 3,3,3-TRIFLUORO-1-NITROPROPENE; 1,1,1-TRICHLORO-3-NITROPROPENE; NUCLEOPHILES; VINYLAMINES

DOI:

10.1016/j.tetlet.2011.04.013

Web of Science ID:

ISI:000291286400028

Соавторы в МНС:

Другие поля

Поле	Значение
Month	JUN 8
Publisher	PERGAMON-ELSEVIER SCIENCE LTD
Address	THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND
Language	English
Keywords-Plus	CYCLIC NITRONIC ESTERS; CYCLOADDITION REACTIONS; CYCLOHEXANONE ENAMINES; N-OXIDE; NITROOLEFINS; OLEFINS; 3,3,3-TRIFLUORO-1-NITROPROPENE; 1,1,1-TRICHLORO-3-NITROPROPENE; NUCLEOPHILES; VINYLAMINES
Research-Areas	Chemistry
Web-of-Science-Categories	Chemistry, Organic
Author-Email	vyacheslav.sosnovskikh@usu.ru
ResearcherID-Numbers	Korotaev, Vladislav/L-2692-2016
ORCID-Numbers	Korotaev, Vladislav/0000-0002-7492-5116
Funding-Acknowledgement	Russian Foundation for Basic Research {[}11-03-00126]
Funding-Text	This work was financially supported by the Russian Foundation for Basic Research (Grant 11-03-00126).
Number-of-Cited-References	43
Usage-Count-Since-2013	10
Journal-ISO	Tetrahedron Lett.
Doc-Delivery-Number	773DE