Unusual Tandem alkynylation and trans-hydrosilylation to form oxasilacyclopentenes

Org Lett. 2005 Oct 27;7(22):4995-8. doi: 10.1021/ol051996r.

Abstract

[reaction: see text] An unusual tandem reaction sequence to form oxasilacyclopentenes from carbonyls and alkynylsilanes in the presence of a catalytic amount of nucleophilic initiator has been discovered. The reaction proceeds readily at room temperature and is applicable to a wide variety of carbonyl substrates. While the reaction scope tolerates variable substitutions on the alkynylsilane, phenylacetylene-derived silane variants consistently achieved the best yield.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Aldehydes / chemistry*
  • Alkynes / chemistry*
  • Cyclopentanes / chemical synthesis*
  • Cyclopentanes / chemistry
  • Ketones / chemistry*
  • Molecular Structure
  • Silanes / chemistry*

Substances

  • Aldehydes
  • Alkynes
  • Cyclopentanes
  • Ketones
  • Silanes