Structure and Computational Basis for Backbone Rearrangement in Marine Oxasqualenoids

J Org Chem. 2021 Feb 5;86(3):2437-2446. doi: 10.1021/acs.joc.0c02600. Epub 2020 Dec 28.

Abstract

Six novel oxasqualenoids (polyether triterpenes) were isolated from the red alga Laurencia viridis. Laurokanols A-E (1-5) comprise an unreported tricyclic core with a [6,6]-spiroketal system. Yucatecone (6) shows a biogenetically intriguing epimerization at C14. Quantum mechanical calculations were used to corroborate their structures and to explain key steps involved in the biogenetic mechanisms proposed for the formation of oxasqualenoids.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Laurencia*
  • Molecular Structure
  • Triterpenes*

Substances

  • Triterpenes