Abstract
Controlled carbometallation of unnactivated acetylenes represents a new methodology in organic synthesis. We have found that the Zr-catalyzed carboalumination of terminal alkynes provides a highly selective and versatile entry into trisubstituted olefins, especially those of terpenoid origin. Its scope, synthetic applications, and mechanism are discussed with emphasis on the cross-coupling reactions of alkenylalanes with organic halides catalyzed by palladium and nickel complexes. © 1981 IUPAC
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CITATION STYLE
Ei-ichi, N. (1981). Bimetallic catalytic systems containing ti, zr, ni, and pd. Their applications to selective organic syntheses. Pure and Applied Chemistry, 53(12), 2333–2356. https://doi.org/10.1351/pac198153122333
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