Lactones 41. Synthesis and microbial hydroxylation of unsaturated terpenoid lactones with p-menthane ring systems

Molecules. 2013 Mar 1;18(3):2778-87. doi: 10.3390/molecules18032778.

Abstract

Racemic [(±)-4-isopropyl-1-methyl-7-oxa-cis-bicyclo[4.3.0]non-4-en-8-one] and optically active δ,ε-unsaturated lactones [(-)-(1R,6R)-4-isopropyl-1-methyl-7-oxabicyclo[4.3.0]non-4-en-8-one and (+)-(1S,6S)-4-isopropyl-1-methyl-7-oxabicyclo[4.3.0] non-4-en-8-one)] with the p-menthane system were obtained and their odoriferous properties were evaluated. Biotransformations of the racemic lactone with three fungal strains: Absidia cylindrospora AM336, Absidia glauca AM177 and Syncephalastrum racemosum AM105, were carried out. Microbial transformations afforded hydroxylactones with the hydroxy group in the allylic position.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biotransformation*
  • Fungi / metabolism
  • Hydroxylation
  • Lactones / chemistry*
  • Lactones / metabolism*
  • Nuclear Magnetic Resonance, Biomolecular
  • Terpenes / chemistry

Substances

  • Lactones
  • Terpenes