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Updated: Apr 13, 2026

Synthesis and Structure Determination of µ-Conotoxin PIIIA Isomers with Different Disulfide Connectivities
Published on: October 2, 2018
Total Synthesis of Gymnocin-A
Takeo Sakai1, Shingo Matsushita1, Shogo Arakawa1
1Faculty of Pharmacy, Meijo University , Yagotoyama 150, Tempaku-ku, Nagoya 468-8503, Japan.
Abstract:
A convergent total synthesis of cytotoxic marine natural polycyclic ether, gymnocin-A (1), is described. The synthesis features three iterations of an oxiranyl anion strategy, involving base-mediated cycloetherification, ring expansion, and reductive etherification, for the construction of the FGH fragment and for its coupling with the ABC and KLMN fragments.
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