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 journalArticle

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 - Jun 27 2001

Fingerprint

Alkylation
Derivatives
aminoindanol
ciguatoxin 3C

All Science Journal Classification (ASJC) codes

  • Organic Chemistry

Cite this

Oishi, T., Tanaka, S. I., Ogasawara, Y., Maeda, K., Oguri, H., & Hirama, M. (2001). Highly stereocontrolled synthesis of the ABCD ring fragment of ciguatoxin CTX3C. Synlett, (SPEC. ISS), 952-954.

Highly stereocontrolled synthesis of the ABCD ring fragment of ciguatoxin CTX3C. / Oishi, T.; Tanaka, S. I.; Ogasawara, Y.; Maeda, K.; Oguri, H.; Hirama, M.

In: Synlett, No. SPEC. ISS, 27.06.2001, p. 952-954.

Research output: Contribution to journalArticle

Oishi, T, Tanaka, SI, Ogasawara, Y, Maeda, K, Oguri, H & Hirama, M 2001, 'Highly stereocontrolled synthesis of the ABCD ring fragment of ciguatoxin CTX3C', Synlett, no. SPEC. ISS, pp. 952-954.
Oishi T, Tanaka SI, Ogasawara Y, Maeda K, Oguri H, Hirama M. Highly stereocontrolled synthesis of the ABCD ring fragment of ciguatoxin CTX3C. Synlett. 2001 Jun 27;(SPEC. ISS):952-954.
Oishi, T. ; Tanaka, S. I. ; Ogasawara, Y. ; Maeda, K. ; Oguri, H. ; Hirama, M. / Highly stereocontrolled synthesis of the ABCD ring fragment of ciguatoxin CTX3C. In: Synlett. 2001 ; No. SPEC. ISS. pp. 952-954.
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