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 |
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ページ(範囲) | 845-846 |
ページ数 | 2 |
ジャーナル | Chemistry Letters |
号 | 9 |
DOI | |
出版ステータス | Published - 1997 1月 1 |
ASJC Scopus subject areas
- 化学 (全般)