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Alkylation of phenol and its derivatives with camphene on large-porous β-zeolite Научная публикация

Журнал Russian Journal of Organic Chemistry
ISSN: 1070-4280 , E-ISSN: 1608-3393
Вых. Данные Год: 2000, Том: 36, Номер: 4, Страницы: 539-552 Страниц : 14
Авторы Fomenko V.V. 1 , Korchagina D.V. 1 , Salakhutdinov N.F. 1 , Bagryanskaya I.Yu. 1 , Gatilov Yu.V. 1 , Ione K.G. 1 , Barkhash V.A. 1
Организации
1 (Scopus) Vorozhtsov Novosibirsk Inst. of O., Siberian Division, Russian Academy of Sciences, Novosibirsk, 630090, Russian Federation

Реферат: Alkylation of phenol, anisole, and their methyl-substituted derivative with camphene catalyzed by large-porous β-zeolite yielded the corresponding terpenylphenols, terpenylanisoles, and terpenyl phenyl ethers. C- or O-alkylation occurs depending on phenol structure and on the solvent used. At C-alkylation the main reaction product has uncommon structure of the terpene rest with methyl groups in 1, 4,and 7 positions.
Библиографическая ссылка: Fomenko V.V. , Korchagina D.V. , Salakhutdinov N.F. , Bagryanskaya I.Y. , Gatilov Y.V. , Ione K.G. , Barkhash V.A.
Alkylation of phenol and its derivatives with camphene on large-porous β-zeolite
Russian Journal of Organic Chemistry. 2000. V.36. N4. P.539-552. WOS Scopus РИНЦ
Идентификаторы:
Web of science WOS:000089918000013
Scopus 2-s2.0-0034164276
РИНЦ 13345323