Stereochemical Definition of the Natural Product (6R,10R,13R, 14R,16R,17R,19S,20S,21R,24S,25S,28S,30S,32R,33R,34R,36S,37S,39R)-Azaspiracid-3 by Total Synthesis and Comparative Analyses

Angew Chem Int Ed Engl. 2018 Jan 15;57(3):810-813. doi: 10.1002/anie.201711008. Epub 2017 Dec 15.

Abstract

The previously accepted structure of the marine toxin azaspiracid-3 is revised based upon an original convergent and stereoselective total synthesis of the natural product. The development of a structural revision hypothesis, its testing, and corroboration are reported. Synthetic (6R,10R,13R,14R,16R,17R,19S,20S,21R,24S,25S,28S,30S,32R, 33R,34R,36S,37S,39R)-azaspiracid-3 chromatographically and spectroscopically matched naturally occurring azaspiracid-3, whereas the previously assigned 20R epimer did not.

Keywords: azaspiracids; natural products; structure elucidation; total synthesis; toxins.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biological Products / chemical synthesis*
  • Biological Products / chemistry*
  • Carbon-13 Magnetic Resonance Spectroscopy
  • Chromatography, Liquid
  • Furans / chemical synthesis*
  • Furans / chemistry*
  • Mass Spectrometry
  • Molecular Structure
  • Oxidation-Reduction
  • Proton Magnetic Resonance Spectroscopy
  • Pyrans / chemical synthesis*
  • Pyrans / chemistry*
  • Stereoisomerism

Substances

  • Biological Products
  • Furans
  • Pyrans
  • azaspiracid-3