Copper-catalyzed 1,2-addition of α-carbonyl iodides to alkynes

Angew Chem Int Ed Engl. 2015 Jan 19;54(4):1307-11. doi: 10.1002/anie.201410279. Epub 2014 Dec 2.

Abstract

β,γ-Unsaturated ketones are an important class of organic molecules. Herein, copper catalysis has been developed for the synthesis of β-γ-unsaturated ketones through 1,2-addition of α-carbonyl iodides to alkynes. The reactions exhibit wide substrate scope and high functional group tolerance. The reaction products are versatile synthetic intermediates to complex small molecules. The method was applied for the formal synthesis of (±)-trichostatin A, a histone deacetylase inhibitor.

Keywords: 1,2-addition reactions; alkynes; copper; ketones; olefination.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkynes / chemistry*
  • Carbonates / chemistry
  • Catalysis
  • Cesium / chemistry
  • Copper / chemistry*
  • Histone Deacetylase Inhibitors / chemical synthesis
  • Histone Deacetylase Inhibitors / chemistry
  • Hydroxamic Acids / chemical synthesis
  • Hydroxamic Acids / chemistry
  • Iodides / chemistry*
  • Ketones / chemistry
  • Mesylates / chemistry
  • Stereoisomerism

Substances

  • Alkynes
  • Carbonates
  • Histone Deacetylase Inhibitors
  • Hydroxamic Acids
  • Iodides
  • Ketones
  • Mesylates
  • Cesium
  • trichostatin A
  • Copper
  • trifluoromethanesulfonic acid
  • cesium carbonate