A biomimetic total synthesis of (+)-ainsliadimer A

Org Lett. 2010 Oct 1;12(19):4284-7. doi: 10.1021/ol101705j.

Abstract

A protecting group free and biomimetic total synthesis of (+)-ainsliadimer A has been accomplished in 14 steps from α-santonin. The synthesis relies on a hydrogen bonding promoted [4 + 2]-hetero-Diels-Alder dimerization to afford the key homodimer intermediate, which demonstrates the feasibility of using nonenzymatic conditions to achieve the proposed biosynthesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomimetic Materials / chemical synthesis*
  • Hydrogen Bonding
  • Lactones / chemical synthesis*
  • Molecular Structure
  • Sesquiterpenes / chemical synthesis*

Substances

  • Lactones
  • Sesquiterpenes
  • ainsliadimer A