Synthetic approach toward complete structure determination of maitotoxin. stereochemical assignment of the C63-C68 acyclic linkage

Makoto Sasaki, Taro Nonomura, Michio Murata, Kazuo Tachibana

Research output: Contribution to journalArticlepeer-review

39 Citations (Scopus)

Abstract

The relative configuration of carbons within the C63-C68 acyclic linkage of maitotoxin (MTX) was assigned by synthesis of stereodefined model compounds (1a-1d) and their comparison with MTX in 1H and 13C NMR spectra.

Original languageEnglish
Pages (from-to)9007-9010
Number of pages4
JournalTetrahedron Letters
Volume36
Issue number49
DOIs
Publication statusPublished - 1995 Dec 4
Externally publishedYes

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

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