Synthetic studies of yessotoxin: Stereoselective annulation of the CD and JK ring fragments by using Pd(II)-catalyzed cyclization

Hajime Yokoyama*, Genki Moriyama, Kazuki Nishida, Yasuhiro Kusumoto, Kiyoshi Tsuge, Masahiro Miyazawa, Yoshiro Hirai

*この論文の責任著者

研究成果: ジャーナルへの寄稿学術論文査読

4 被引用数 (Scopus)

抄録

Yessotoxin is the polycyclic ether implicated in diarrheic shellfish poisoning. This toxin has A-K ring system involving 6-, 7-, 8-membered ether rings. We have been studying high stereoselective Pd(II)-catalyzed cyclization. Herein we describe the CD and JK ring fragments of yessotoxin by our annulation based on Pd(II)-catalyzed cyclization. The efforts to understand these high stereoselectivities are also disclosed. This annulation method could be applicable to other polyethers and related natural products.

本文言語英語
ページ(範囲)470-482
ページ数13
ジャーナルHeterocycles
96
3
DOI
出版ステータス出版済み - 2018

ASJC Scopus 主題領域

  • 有機化学
  • 創薬

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