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Эта публикация цитируется в 1 научной статье (всего в 1 статье)
Selectivity of the Lewis acid-induced transformations of polyfunctional compounds containing a 4,6-dialkoxy-7-(arylthio)heptene moiety
D. S. Chekmareva, A. V. Maskaeva, G. V. Zatonskyb, M. I. Lazarevaa, R. Caplec, W. A. Smitb a Higher Chemical College of the Russian Academy of Sciences, D.I. Mendeleev University of Chemical Technology of Russia, Moscow, Russian Federation
b N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
c Department of Chemistry, University of Minnesota Duluth, Duluth, Minnesota, USA
Аннотация:
The interaction of the title adducts with Lewis acids may proceed as an attack at either β-alkoxy or δ-alkoxy group to the arylthio substituent leading to the formation of substituted cyclohexane or 1,3-diene derivatives, respectively.
Образец цитирования:
D. S. Chekmarev, A. V. Maskaev, G. V. Zatonsky, M. I. Lazareva, R. Caple, W. A. Smit, “Selectivity of the Lewis acid-induced transformations of polyfunctional compounds containing a 4,6-dialkoxy-7-(arylthio)heptene moiety”, Mendeleev Commun., 11:5 (2001), 176–178
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc4280 https://www.mathnet.ru/rus/mendc/v11/i5/p176
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