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This article is cited in 12 scientific papers (total in 12 papers)
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
Abstract:
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.
Citation:
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
Linking options:
https://www.mathnet.ru/eng/mendc5022 https://www.mathnet.ru/eng/mendc/v5/i2/p41
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