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

Журнал Mendeleev Communications
ISSN: 0959-9436
Вых. Данные Год: 1992, Том: 2, Номер: 3, Страницы: 82-83 Страниц : 2 DOI: 10.1070/MC1992v002n03ABEH000142
Авторы Chibiryaev Andrei M. 1 , Bagryanskaya Irina Yu. 1 , Gatilov Yurii V. 1 , Tkachev Aleksei V. 1
Организации
1 (Scopus) Novosibirsk Institute of Organic Chemistry, Siberian Branch, Russian Academy of Sciences, Novosibirsk, 630090, Russian Federation

Реферат: 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.
Библиографическая ссылка: 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
Даты:
Опубликована в печати: 1 янв. 1992 г.
Идентификаторы БД:
Web of science: WOS:A1992JG80600002
Scopus: 2-s2.0-85025349759
РИНЦ: 31074761
OpenAlex: W2029411611
Цитирование в БД:
БД Цитирований
OpenAlex 1
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