Convergent strategy for synthesizing polycyclic ether marine toxins: Synthesis of the ABCDE ring fragment of ciguatoxin CTX3C

Megumi Maruyama, Kenji Maeda, Tohru Oishi, Hiroki Oguri, Masahiro Hirama

Research output: Contribution to journalArticle

36 Citations (Scopus)

Abstract

The ABCDE ring fragment of CTX3C, the most important member of the ciguatoxin family, was concisely synthesized by extensive use of ring-closing olefin metathesis.

Original languageEnglish
Pages (from-to)93-99
Number of pages7
JournalHeterocycles
Volume54
Issue number1
Publication statusPublished - Jan 1 2001

Fingerprint

Ciguatoxins
Marine Toxins
Alkenes
Ether
ciguatoxin 3C

All Science Journal Classification (ASJC) codes

  • Analytical Chemistry
  • Pharmacology
  • Organic Chemistry

Cite this

Convergent strategy for synthesizing polycyclic ether marine toxins : Synthesis of the ABCDE ring fragment of ciguatoxin CTX3C. / Maruyama, Megumi; Maeda, Kenji; Oishi, Tohru; Oguri, Hiroki; Hirama, Masahiro.

In: Heterocycles, Vol. 54, No. 1, 01.01.2001, p. 93-99.

Research output: Contribution to journalArticle

Maruyama, Megumi ; Maeda, Kenji ; Oishi, Tohru ; Oguri, Hiroki ; Hirama, Masahiro. / Convergent strategy for synthesizing polycyclic ether marine toxins : Synthesis of the ABCDE ring fragment of ciguatoxin CTX3C. In: Heterocycles. 2001 ; Vol. 54, No. 1. pp. 93-99.
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