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Эта публикация цитируется в 12 научных статьях (всего в 12 статьях)
A Convenient Protocol for the Stereocontrolled Synthesis of Olefins with a Homoallylic Type of Functionality
A. A. Vasil'ev, G. V. Kryshtal', E. P. Serebryakov
N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
Аннотация:
A combination of the Homer–Emmons synthesis of alkyl 2,4-dienoates with their hydrogenation over complex L·Cr(CO)3 catalysts (L = arene or 3CO) provides a versatile, stereocontrolled approach to olefins with a homoallylic pattern of functional substitution, such as certain insect pheromones or (Z)-prenylated arenes analogous to the “left-side” moiety of bifurcarenone.
Образец цитирования:
A. A. Vasil'ev, G. V. Kryshtal', E. P. Serebryakov, “A Convenient Protocol for the Stereocontrolled Synthesis of Olefins with a Homoallylic Type of Functionality”, Mendeleev Commun., 5:2 (1995), 41–42
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc5022 https://www.mathnet.ru/rus/mendc/v5/i2/p41
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