Oxidative degradations of the side chain of unsaturated ent-labdanes. Part II

Molecules. 2007 Dec 21;12(12):2605-20. doi: 10.3390/12122605.

Abstract

A route for the degradation of the side chain of ent-labdane derivatives has been devised, giving the useful synthon 2beta,12-dihydroxy-13,14,15,16,17-pentanor-ent-labdane-8-one (8). The use of this compound in the preparation of terpenylquinone derivatives shall be reported elsewhere. In addition we have synthesized the compound 2beta,12-diacetoxy-8beta,17-epoxy-13,14,15,16-tetranor-ent-labdane (10), which upon catalytic epoxide ring opening in alkaline or acid media gave rise in all cases to the formation of tricyclicc ompounds.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Diterpenes / chemistry*
  • Diterpenes / metabolism*
  • Magnetic Resonance Spectroscopy
  • Models, Molecular
  • Oxidation-Reduction

Substances

  • Diterpenes