Concise enantioselective total synthesis of neopeltolide macrolactone highlighted by ether transfer

Org Lett. 2008 Nov 6;10(21):5047-50. doi: 10.1021/ol802254z. Epub 2008 Oct 15.

Abstract

A concise total synthesis of neopeltolide macrolactone has been accomplished in 14 steps in the longest linear sequence, 15 steps overall from commercially available materials. The present synthesis was highlighted by successful exploitation of ether transfer methodology and a radical cyclization reaction to directly establish the requisite stereochemistry of the tetrahydropyran core.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Ether / chemistry*
  • Macrolides / chemical synthesis*
  • Macrolides / chemistry
  • Molecular Structure
  • Stereoisomerism

Substances

  • Macrolides
  • neopeltolide
  • Ether