Allylation and Alkylation of Biologically Relevant Nucleophiles by Diallyl Sulfides

J Org Chem. 2017 Jan 6;82(1):776-780. doi: 10.1021/acs.joc.6b02517. Epub 2016 Dec 14.

Abstract

Allyl sulfides are bioactive phytochemicals found in garlic, onion, and other members of the genus Allium. Here we showed that diallyl disulfide and diallyl trisulfide can transfer allyl side chains to low molecular weight thiols. Diallyl monosulfide is inert with respect to this allyl transfer reaction. On the other hand, diallyl sulfone, a known metabolite of diallyl monosulfide, alkylates both amines and thiols under physiologically relevant conditions via isomerization to an electrophilic vinyl sulfone.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Alkylation
  • Allium / chemistry*
  • Allyl Compounds / chemical synthesis*
  • Allyl Compounds / chemistry*
  • Disulfides / chemistry*
  • Molecular Structure
  • Sulfides / chemical synthesis*
  • Sulfides / chemistry*

Substances

  • Allyl Compounds
  • Disulfides
  • Sulfides
  • diallyl trisulfide
  • diallyl disulfide
  • allyl sulfide