Highly stereocontrolled synthesis of the ABCD ring fragment of ciguatoxin CTX3C

T. Oishi, S. I. Tanaka, Y. Ogasawara, K. Maeda, H. Oguri, M. Hirama

Research output: Contribution to journalArticlepeer-review

28 Citations (Scopus)

Abstract

A combination of asymmetric alkylation using (1R,2S)-1-amino-2-indanol derivative as a chiral auxiliary and the ring-closing metathesis reaction was shown to be an efficient method for synthesizing the ABCD ring fragment of ciguatoxin CTX3C.

Original languageEnglish
Pages (from-to)952-954
Number of pages3
JournalSynlett
Issue numberSPEC. ISS
Publication statusPublished - 2001 Jun 27

Keywords

  • Asymmetric alkylation
  • Ciguatoxin CTX3C
  • Multiple asymmetric induction
  • Polycyclic ether
  • Ring-closing metathesis

ASJC Scopus subject areas

  • Organic Chemistry

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