Versatile and efficient synthesis of omega-functionalized asymmetric disulfides via sulfenyl bromide adducts

Langmuir. 2007 Feb 27;23(5):2318-21. doi: 10.1021/la063013k. Epub 2007 Jan 24.

Abstract

Various types of asymmetric disulfides can be synthesized under mild conditions and in excellent yields by a method involving dialkoxylthiophosphoranesulfenyl halide precursors. This straightforward, rapid procedure is used to prepare a series of disulfides bearing neutral, acidic, and basic terminal groups as well as groups commonly used in biospecific self-assembled monolayers.

Publication types

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

MeSH terms

  • Bromides / chemistry*
  • Catalysis
  • Chemistry, Physical / methods*
  • Disulfides / chemistry*
  • Electrochemistry / methods
  • Models, Chemical
  • Molecular Structure

Substances

  • Bromides
  • Disulfides