Stereoselective Synthesis of the LM Ring Moiety of Ciguatoxin : Reagent Control of Asymmetric Dihydroxylation

この論文にアクセスする

この論文をさがす

著者

    • OISHI Tohru
    • Department of Chemistry, Graduate School of Science, Tohoku University
    • SHOJI Mitsuru
    • Department of Chemistry, Graduate School of Science, Tohoku University
    • KUMAHARA Naomi
    • Department of Chemistry, Graduate School of Science, Tohoku University
    • HIRAMA Masahiro
    • Department of Chemistry, Graduate School of Science, Tohoku University

抄録

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

収録刊行物

  • Chemistry letters  

    Chemistry letters 1997(9), 845-846, 1997-09 

    The Chemical Society of Japan

参考文献:  20件

参考文献を見るにはログインが必要です。ユーザIDをお持ちでない方は新規登録してください。

各種コード

  • NII論文ID(NAID)
    10002614489
  • NII書誌ID(NCID)
    AA00603318
  • 本文言語コード
    ENG
  • 資料種別
    ART
  • ISSN
    03667022
  • データ提供元
    CJP書誌  J-STAGE 
ページトップへ