Direct preparation of nucleoside vinyl disulfides from 2-(trimethylsilyl)ethyl sulfides, an access to vinylthiols

Org Lett. 2007 Aug 2;9(16):3021-3. doi: 10.1021/ol071088p. Epub 2007 Jul 4.

Abstract

We report here a straightforward preparation of various nucleoside vinyl disulfides in high yields under mild conditions using the new reaction of vinyl 2-(trimethylsilyl)ethyl (TMSE) sulfides with sulfenyl chlorides. This reaction allows the preparation of various mixed disulfides from stable silyl sulfides without formation of oxidizable and/or unstable thiols. The easy preparation of vinyl disulfides through this reaction should offer new perspectives in vinylthiol chemistry.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Disulfides / chemical synthesis*
  • Disulfides / chemistry
  • Molecular Structure
  • Nucleosides / chemical synthesis*
  • Nucleosides / chemistry
  • Silanes / chemistry
  • Sulfhydryl Compounds / chemical synthesis*
  • Sulfhydryl Compounds / chemistry
  • Sulfides / chemistry
  • Vinyl Compounds / chemical synthesis*
  • Vinyl Compounds / chemistry

Substances

  • Disulfides
  • Nucleosides
  • Silanes
  • Sulfhydryl Compounds
  • Sulfides
  • Vinyl Compounds