Catalytic asymmetric claisen rearrangement in natural product synthesis: synthetic studies toward (-)-xeniolide F

Org Lett. 2005 Dec 8;7(25):5705-8. doi: 10.1021/ol052462t.

Abstract

[chemical reaction: see text]. The catalytic asymmetric Claisen rearrangement (CAC) of a highly substituted and functionalized alpha-alkoxycarbonyl-substituted allyl vinyl ether has been exploited to gain access to an advanced building block for the projected total synthesis of (-)-xeniolide F, the enantiomer of a xenicane diterpene isolated from a coral of the genus Xenia.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anthozoa / chemistry
  • Catalysis
  • Diterpenes / chemical synthesis*
  • Diterpenes / chemistry
  • Molecular Structure
  • Stereoisomerism
  • Vinyl Compounds / chemistry*

Substances

  • Diterpenes
  • Vinyl Compounds
  • xeniolide F
  • vinyl ether