Visible-Light-Driven, Copper-Catalyzed Decarboxylative C(sp3 )-H Alkylation of Glycine and Peptides

Angew Chem Int Ed Engl. 2018 Nov 26;57(48):15841-15846. doi: 10.1002/anie.201809400. Epub 2018 Nov 7.

Abstract

Despite a well-developed and growing body of work in Cu catalysis, the potential of Cu to serve as a photocatalyst remains underexplored. Reported herein is the first example of visible-light-induced Cu-catalyzed decarboxylative C(sp3 )-H alkylation of glycine for preparing α-alkylated unnatural α-amino acids. It merits mentioning that the mild conditions and the good functional-group tolerance allow the modification of peptides using this method. The mechanistic studies revealed that a radical-radical coupling pathway is involved in the reaction.

Keywords: copper; cross-coupling; peptides; photochemistry; radicals.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkylation
  • Amino Acids / chemical synthesis*
  • Amino Acids / chemistry
  • Catalysis
  • Copper / chemistry*
  • Decarboxylation
  • Glycine / chemistry*
  • Light*
  • Molecular Structure
  • Peptides / chemistry*

Substances

  • Amino Acids
  • Peptides
  • Copper
  • Glycine