Diversity-oriented synthesis of disubstituted alkenes using masked silanols

Org Lett. 2010 Jun 18;12(12):2806-9. doi: 10.1021/ol100895d.

Abstract

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkenes / chemical synthesis*
  • Alkenes / chemistry
  • Alkynes / chemistry*
  • Catalysis
  • Combinatorial Chemistry Techniques
  • Hydrocarbons, Fluorinated / chemical synthesis
  • Hydrocarbons, Fluorinated / chemistry
  • Molecular Structure
  • Silanes / chemical synthesis
  • Silanes / chemistry*
  • Stereoisomerism

Substances

  • Alkenes
  • Alkynes
  • Hydrocarbons, Fluorinated
  • Silanes
  • silanol