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

Tohru Oishi, Mitsuru Shoji, Naomi Kumahara, Masahiro Hirama

研究成果: ジャーナルへの寄稿記事

34 引用 (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.

元の言語英語
ページ(範囲)845-846
ページ数2
ジャーナルChemistry Letters
発行部数9
DOI
出版物ステータス出版済み - 1 1 1997
外部発表Yes

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Ciguatoxins
Alkenes

All Science Journal Classification (ASJC) codes

  • Chemistry(all)

これを引用

Stereoselective synthesis of the LM ring moiety of ciguatoxin : Reagent control of asymmetric dihydroxylation. / Oishi, Tohru; Shoji, Mitsuru; Kumahara, Naomi; Hirama, Masahiro.

:: Chemistry Letters, 番号 9, 01.01.1997, p. 845-846.

研究成果: ジャーナルへの寄稿記事

Oishi, Tohru ; Shoji, Mitsuru ; Kumahara, Naomi ; Hirama, Masahiro. / Stereoselective synthesis of the LM ring moiety of ciguatoxin : Reagent control of asymmetric dihydroxylation. :: Chemistry Letters. 1997 ; 番号 9. pp. 845-846.
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