Аннотация:
The stereoselectivity of the formation of cis-3,4-dihydronaphthalenes from 1-styryl substituted isochromenes proves the intermediacy of O-quinodimethanes in this reaction.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
S. V. Verin, D. E. Tosunyan, E. V. Kuznetsov, “An Efficient Access to α-Tetralones and their Derivatives via O-Quinodimethanes Generated by Isochromene Ring Cleavage”, Mendeleev Commun., 2:1 (1992), 20–21
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc5375
https://www.mathnet.ru/rus/mendc/v2/i1/p20
Эта публикация цитируется в следующих 2 статьяx:
Ye Bao, Dawei Yue, Nicola Della Cà, Richard C. Larock, Daniel W. Armstrong, “Enantiomeric Separation of Isochromene Derivatives by Cyclodextrin-Modified Micellar Capillary Electrophoresis”, Journal of Liquid Chromatography & Related Technologies, 31:14 (2008), 2035
S. V. VERIN, D. E. TOSUNYAN, E. V. KUZNETSOV, “ChemInform Abstract: An Efficient Access to α‐Tetralones and Their Derivatives via O‐ Quinodimethanes Generated by Isochromene Ring Cleavage.”, ChemInform, 23:39 (1992)
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