Stereoselective synthesis of the LM ring moiety of ciguatoxin: Reagent control of asymmetric dihydroxylation

Tohru Oishi; Mitsuru Shoji; Naomi Kumahara; Masahiro Hirama

doi:10.1246/cl.1997.845

Stereoselective synthesis of the LM ring moiety of ciguatoxin: Reagent control of asymmetric dihydroxylation

Tohru Oishi, Mitsuru Shoji, Naomi Kumahara, Masahiro Hirama

薬科学科

研究成果: Article › 査読

37 被引用数 (Scopus)

抄録

Stereoselective synthesis of the LM ring moiety of ciguatoxin was achieved from (R)-(E)-1-benzyloxy-2-hydroxy-3-pentene via Ireland-Claisen rearrangement, iodolactonization, and reagent-controlled asymmetric dihydroxylation.

本文言語	English
ページ（範囲）	845-846
ページ数	2
ジャーナル	Chemistry Letters
号	9
DOI	https://doi.org/10.1246/cl.1997.845
出版ステータス	Published - 1997 1月 1

ASJC Scopus subject areas

化学 (全般)

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10.1246/cl.1997.845

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Stereoselective synthesis of the LM ring moiety of ciguatoxin: Reagent control of asymmetric dihydroxylation

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