General and practical formation of thiocyanates from thiols

Chemistry. 2015 Feb 2;21(6):2662-8. doi: 10.1002/chem.201406171. Epub 2014 Dec 17.

Abstract

A new method for the cyanation of thiols and disulfides using cyanobenziodoxol(on)e hypervalent iodine reagents is described. Both aliphatic and aromatic thiocyanates can be accessed in good yields in a few minutes at room temperature starting from a broad range of thiols with high chemioselectivity. The complete conversion of disulfides to thiocyanates was also possible. Preliminary computational studies indicated a low energy concerted transition state for the cyanation of the thiolate anion or radical. The developed thiocyanate synthesis has broad potential for various applications in synthetic chemistry, chemical biology and materials science.

Keywords: chemoselectivity; cyanation; hypervalent iodine; synthetic methods; thiocyanates.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Iodine / chemistry
  • Isomerism
  • Molecular Conformation
  • Sulfhydryl Compounds / chemistry*
  • Thermodynamics
  • Thiocyanates / chemical synthesis
  • Thiocyanates / chemistry*

Substances

  • Sulfhydryl Compounds
  • Thiocyanates
  • Iodine
  • thiocyanate