An Unusual Dimerization in the Nitrosation Reaction of a Caryophyllene-type α,β-Unsaturated Oxime

An Unusual Dimerization in the Nitrosation Reaction of a Caryophyllene-type α,β-Unsaturated Oxime Full article

Journal

Mendeleev Communications
ISSN: 0959-9436

Output data

Year: 1992, Volume: 2, Number: 3, Pages: 82-83 Pages count : 2 DOI: 10.1070/MC1992v002n03ABEH000142

Authors

Chibiryaev Andrei M. ¹ , Bagryanskaya Irina Yu. ¹ , Gatilov Yurii V. ¹ , Tkachev Aleksei V. ¹

Affiliations

1	(Scopus) Novosibirsk Institute of Organic Chemistry, Siberian Branch, Russian Academy of Sciences, Novosibirsk, 630090, Russian Federation

The treatment of two isomeric α,β-unsaturated oximes derived from the sesquiterpene hydrocarbon caryophyllene with nitrous acid, generated in situ from sodium nitrite and acetic acid, results in the formation of an unusual dimeric product whose structure was determined by X-ray crystallographic analysis. © 1992, jointly by The Russian Academy of Sciences and The Royal Society of Chemistry (Turpion Ltd). All rights reserved.

Chibiryaev A.M. , Bagryanskaya I.Y. , Gatilov Y.V. , Tkachev A.V.
An Unusual Dimerization in the Nitrosation Reaction of a Caryophyllene-type α,β-Unsaturated Oxime
Mendeleev Communications. 1992. V.2. N3. P.82-83. DOI: 10.1070/MC1992v002n03ABEH000142 WOS Scopus РИНЦ OpenAlex

Published print:

Jan 1, 1992

Web of science:	WOS:A1992JG80600002
Scopus:	2-s2.0-85025349759
Elibrary:	31074761
OpenAlex:	W2029411611

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