Total synthesis of (-)-aritasone via the ultra-high pressure hetero-Diels-Alder dimerisation of (-)-pinocarvone

Org Biomol Chem. 2017 Oct 18;15(40):8523-8528. doi: 10.1039/c7ob02204b.

Abstract

This paper describes a total synthesis of the terpene-derived natural product aritasone via the hetero-Diels-Alder [4 + 2] cyclodimerisation of pinocarvove, which represents the proposed biosyntheic route. The hetero-Diels-Alder dimerisation of pinocarvone did not proceed under standard conditions, and ultra-high pressure (19.9 kbar) was required. As it seems unlikely that these ultra-high pressures are accessible within a plant cell, we suggest that the original biosynthetic hypothesis be reconsidered, and alternatives are discussed.

MeSH terms

  • Bicyclic Monoterpenes
  • Cycloaddition Reaction
  • Dimerization
  • Molecular Conformation
  • Monoterpenes / chemistry*
  • Pressure
  • Stereoisomerism

Substances

  • Bicyclic Monoterpenes
  • Monoterpenes
  • pinocarvone