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Identification of the absolute configuration of pectenotoxin-6, a polyether macrolide compound, by NMR spectroscopic method using a chiral anisotropic reagent, phenylglycine methyl ester.

Abstract
The absolute configuration of pectenotoxin-6 (4, PTX6), found in association with diarrhetic shellfish poisoning, was identified by NMR spectroscopy using a chiral anisotropic reagent, phenylglycine methyl ester (PGME), which was condensed with a carboxyl group of 4.
AuthorsK Sasaki, M Satake, T Yasumoto
JournalBioscience, biotechnology, and biochemistry (Biosci Biotechnol Biochem) Vol. 61 Issue 10 Pg. 1783-5 (Oct 1997) ISSN: 0916-8451 [Print] England
PMID9362128 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Furans
  • Macrolides
  • Marine Toxins
  • Pyrans
  • pectenotoxin 6
  • methyl phenylglycine
  • Glycine
Topics
  • Furans (chemistry)
  • Glycine (analogs & derivatives)
  • Macrolides
  • Magnetic Resonance Spectroscopy
  • Marine Toxins (chemistry)
  • Pyrans (chemistry)
  • Stereoisomerism

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