I2-catalyzed regioselective oxo- and hydroxy-acyloxylation of alkenes and enol ethers: a facile access to α-acyloxyketones, esters, and diol derivatives

Org Lett. 2014 Nov 7;16(21):5674-7. doi: 10.1021/ol5027393. Epub 2014 Oct 29.

Abstract

I2-catalyzed oxo-acyloxylation of alkenes and enol ethers with carboxylic acids providing for the high yield synthesis of α-acyloxyketones and esters is described. This unprecedented regioselective oxidative process employs TBHP and Et3N in stoichiometric amounts under metal-free conditions in DMSO as solvent. Additionally, I2-catalysis allows the direct hydroxy-acyloxylation of alkenes with the sequential addition of BH3·SMe2 leading to monoprotected diol derivatives in excellent yields.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkenes / chemistry*
  • Carboxylic Acids / chemistry*
  • Catalysis
  • Dimethyl Sulfoxide / chemistry*
  • Esters
  • Ethers / chemistry*
  • Ketones / chemical synthesis*
  • Ketones / chemistry
  • Oxidation-Reduction
  • Solvents / chemistry
  • Stereoisomerism

Substances

  • Alkenes
  • Carboxylic Acids
  • Esters
  • Ethers
  • Ketones
  • Solvents
  • Dimethyl Sulfoxide