Oxonium ylide rearrangement of enzymatically desymmetrized glutarates

Org Lett. 2013 Dec 6;15(23):5998-6001. doi: 10.1021/ol402887z. Epub 2013 Nov 7.

Abstract

The combination of an enzyme-mediated enantioselective desymmetrization of readily available 3-benzyloxyglutarates and subsequent rhodium-catalyzed oxonium ylide rearrangement of their corresponding in situ derived diazo ketones offers a very concise and highly stereoselective access to functionalized tetrahydrofuranone building blocks.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Furans / chemical synthesis*
  • Furans / chemistry
  • Glutarates / chemistry*
  • Molecular Structure
  • Onium Compounds / chemistry*
  • Rhodium / chemistry*
  • Stereoisomerism

Substances

  • Furans
  • Glutarates
  • Onium Compounds
  • hydronium ion
  • Rhodium