Extensive Ring-Expansion Strategy for the Enantioselective Synthesis of the Medium Ring Ethers, Oxepene, Oxocane, and Oxonene, of Ciguatoxin

Tohru Oishi, Mitsuru Shoji, Kenji Maeda, Naomi Kumahara, Masahiro Hirama

研究成果: Article査読

44 被引用数 (Scopus)

抄録

The extensive ring-expansion strategy for the synthesis of oxepene 19, oxocane 23, and oxonene 28, which correspond to the D (E), I and F ring fragments of ciguatoxin (1), respectively, has been established. Chemoenzymatic asymmetric acylation of the meso alcohols using lipase AK provided a simple entry of the enantiomeric building blocks.

本文言語English
ページ(範囲)1165-1167
ページ数3
ジャーナルSynlett
1996
12
DOI
出版ステータスPublished - 1996
外部発表はい

ASJC Scopus subject areas

  • 有機化学

フィンガープリント

「Extensive Ring-Expansion Strategy for the Enantioselective Synthesis of the Medium Ring Ethers, Oxepene, Oxocane, and Oxonene, of Ciguatoxin」の研究トピックを掘り下げます。これらがまとまってユニークなフィンガープリントを構成します。

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