Stereocontrolled synthesis of the HIJ ring system of ciguatoxin

Tohru Oishi, Kenji Maeda, Masahiro Hirama

Research output: Contribution to journalArticle

36 Citations (Scopus)

Abstract

Divergent synthesis of the HIJ ring framework 21 of ciguatoxin 1 starting with oxocane 10 is achieved using the palladium- and acid-catalysed cyclization reactions of hydroxy epoxides.

Original languageEnglish
Pages (from-to)1289-1290
Number of pages2
JournalChemical Communications
Issue number14
DOIs
Publication statusPublished - Jan 1 1997

Fingerprint

Ciguatoxins
Cyclization
Epoxy Compounds
Palladium
Acids

All Science Journal Classification (ASJC) codes

  • Catalysis
  • Electronic, Optical and Magnetic Materials
  • Ceramics and Composites
  • Chemistry(all)
  • Surfaces, Coatings and Films
  • Metals and Alloys
  • Materials Chemistry

Cite this

Stereocontrolled synthesis of the HIJ ring system of ciguatoxin. / Oishi, Tohru; Maeda, Kenji; Hirama, Masahiro.

In: Chemical Communications, No. 14, 01.01.1997, p. 1289-1290.

Research output: Contribution to journalArticle

Oishi, Tohru ; Maeda, Kenji ; Hirama, Masahiro. / Stereocontrolled synthesis of the HIJ ring system of ciguatoxin. In: Chemical Communications. 1997 ; No. 14. pp. 1289-1290.
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