Biomimetic cyclization of geraniol derivatives, a useful tool in the total synthesis of bioactive monocyclic terpenoids

Nat Prod Commun. 2011 Apr;6(4):465-76.

Abstract

This review is a detailed account of authors' work in the field of biomimetic cyclization of geraniol-like dienes. The very high regio- and enantioselectivity achieved made these elegant reactions a viable tool for the synthesis of monocyclic building blocks used in the synthesis of valued terpenoids, like the precious aroma and perfume constituents' ionones and irones.

Publication types

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

MeSH terms

  • Acyclic Monoterpenes
  • Biomimetics*
  • Cyclization
  • Stereoisomerism
  • Terpenes / chemical synthesis*
  • Terpenes / chemistry

Substances

  • Acyclic Monoterpenes
  • Terpenes
  • geraniol