Highly stereocontrolled synthesis of the ABCD ring fragment of ciguatoxin CTX3C

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

Highly stereocontrolled synthesis of the ABCD ring fragment of ciguatoxin CTX3C

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

研究成果: Contribution to journal › Article › 査読

抄録

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.

本文言語	英語
ページ（範囲）	952-954
ページ数	3
ジャーナル	Synlett
号	SPEC. ISS
出版ステータス	出版済み - 6 27 2001
外部発表	はい

All Science Journal Classification (ASJC) codes

Organic Chemistry

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引用スタイル

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title = "Highly stereocontrolled synthesis of the ABCD ring fragment of ciguatoxin CTX3C",

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.",

author = "T. Oishi and Tanaka, {S. I.} and Y. Ogasawara and K. Maeda and H. Oguri and M. Hirama",

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T1 - Highly stereocontrolled synthesis of the ABCD ring fragment of ciguatoxin CTX3C

AU - Oishi, T.

AU - Tanaka, S. I.

AU - Ogasawara, Y.

AU - Maeda, K.

AU - Oguri, H.

AU - Hirama, M.

PY - 2001/6/27

Y1 - 2001/6/27

N2 - 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.

AB - 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.

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