Chemical Synthesis of the GHIJKLMNO Ring System of Maitotoxin

J Am Chem Soc. 2008 Jun 11;130(23):7466-76. doi: 10.1021/ja801139f. Epub 2008 May 16.

Abstract

As the largest secondary metabolite to be discovered as of yet, the polyether marine neurotoxin maitotoxin constitutes a major structural and synthetic challenge. After its originally proposed structure ( 1) had been questioned on the basis of biosynthetic considerations, we provided computational and experimental support for structure 1. In an effort to provide stronger experimental evidence of the molecular architecture of maitotoxin, its GHIJKLMNO ring system 3 was synthesized. The (13)C NMR chemical shifts of synthetic 3 matched closely those corresponding to the same domain of the natural product providing strong evidence for the correctness of the originally proposed structure of maitotoxin ( 1).

Publication types

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

MeSH terms

  • Carbohydrates / chemistry
  • Carbon Isotopes
  • Furans / chemistry
  • Marine Toxins / chemical synthesis*
  • Nuclear Magnetic Resonance, Biomolecular
  • Oxocins / chemical synthesis*

Substances

  • Carbohydrates
  • Carbon Isotopes
  • Furans
  • Marine Toxins
  • Oxocins
  • maitotoxin