How a diversity-oriented approach has inspired a new hypothesis for the gabosine biosynthetic pathway. A new synthesis of (+)-gabosine C

Org Biomol Chem. 2013 Oct 14;11(38):6562-8. doi: 10.1039/c3ob41183d. Epub 2013 Aug 28.

Abstract

A new synthesis of (+)-gabosine C has been accomplished as part of a general diversity-oriented approach that also delivered the previously unknown (-)-4-epi-gabosine C. The identification of the unexpected intermediate (+)-8, together with the isolation of ketones 9 and 10 in previous investigations, prompted us to formulate a new hypothesis for the biosynthesis of gabosines, based on a keto-enol equilibrium cascade pathway starting from 2-epi-5-epi-valiolone, along which the necessary precursors for all the different types of gabosines are generated.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cyclohexanols / chemical synthesis*
  • Cyclohexanols / chemistry
  • Cyclohexanols / metabolism
  • Cyclohexanones / chemical synthesis*
  • Cyclohexanones / chemistry
  • Cyclohexanones / metabolism
  • Ketones / chemistry*
  • Molecular Structure
  • Stereoisomerism

Substances

  • Cyclohexanols
  • Cyclohexanones
  • Ketones
  • KD 16U1