4.8 Article

Diversity-Oriented Synthesis of Disubstituted Alkenes Using Masked Silanols

Journal

ORGANIC LETTERS
Volume 12, Issue 12, Pages 2806-2809

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol100895d

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Funding

  1. EPSRC
  2. BBSRC
  3. GlaxoSmithKline

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The regio- and stereoselective synthesis and subsequent Hiyama cross coupling of pentafluorophenyldimethylvinylsilanes has been developed, thus providing a convenient and robust method for the diversity-oriented synthesis of (E)-, (Z)- and alpha-disubstituted alkenes from terminal alkynes. Pentafluorophenyldimethylvinylsilanes undergo cross-coupling reactions with excellent selectivity and in good yields, offering an attractive alternative to existing masked silanols.

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