Enantioselective synthesis of a hydroxymethyl-cis-1,3-cyclopentenediol building block

Org Lett. 2012 Nov 16;14(22):5716-9. doi: 10.1021/ol3027297. Epub 2012 Oct 26.

Abstract

A brief, enantioselective synthesis of a hydroxymethyl-cis-1,3-cyclopentenediol building block is presented. This scaffold allows access to the cis-1,3-cyclopentanediol fragments found in a variety of biologically active natural and non-natural products. This rapid and efficient synthesis is highlighted by the utilization of the palladium-catalyzed enantioselective allylic alkylation of dioxanone substrates to prepare tertiary alcohols.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alcohols / chemical synthesis*
  • Alcohols / chemistry
  • Alkylation
  • Catalysis
  • Cyclopentanes / chemical synthesis*
  • Cyclopentanes / chemistry
  • Dioxanes / chemistry*
  • Molecular Structure
  • Palladium / chemistry*
  • Stereoisomerism

Substances

  • Alcohols
  • Cyclopentanes
  • Dioxanes
  • Palladium