Lewis acid catalyzed highly regio- and stereocontrolled trans- hydrosilylation of alkynes and allenes

T. Sudo, Naoki Asao, V. Gevorgyan, Y. Yamamoto

    Research output: Contribution to journalArticlepeer-review

    105 Citations (Scopus)

    Abstract

    Lewis acids such as AlCl3 or EtAlCl2 dramatically catalyzed the hydrosilylation of alkynes 1 with trialkylsilanes to produce the corresponding cis-vinylsilanes 2 in a regio- and trans-stereoselective manner. For example, the hydrosilylation of 1-dodecyne 1a with triethylsilane in the presence of 0.2 equiv of AlCl3 gave cis-1-(triethylsilyl)-1-dodecene in 93% yield. Other alkyl- and phenyl-substituted terminal and internal acetylenes also underwent trans-hydrosilylation very smoothly. In the case of alkoxy- or silyloxy-substituted acetylenes, the use of 1.2 equiv of AlCl3 or EtAlCl2 was essential to obtain the corresponding trans-hydrosilylation products in high yields. Moreover, AlCl3 catalyzed the hydrosilylation of aromatic allenes 11, producing the alkenylsilanes 12 with high regio- and stereoselectivities in moderate to high chemical yields. Not only the simple monosubstituted, but also the disubstituted and trisubstituted allenes, underwent the hydrosilylation reaction smoothly, serving as a useful tool for the synthesis of differently substituted vinylsilanes which are not easily available through the previously known methodologies. The mechanisms for these catalytic reactions of alkynes and allenes are proposed.

    Original languageEnglish
    Pages (from-to)2494-2499
    Number of pages6
    JournalJournal of Organic Chemistry
    Volume64
    Issue number7
    DOIs
    Publication statusPublished - 1999 Apr 2

    ASJC Scopus subject areas

    • Organic Chemistry

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