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Updated: May 17, 2026

Synthesis and Structure Determination of µ-Conotoxin PIIIA Isomers with Different Disulfide Connectivities
Published on: October 2, 2018
Synthesis of the C1-C26 hexacyclic subunit of pectenotoxin 2
Ozora Kubo1, Daniel P Canterbury, Glenn C Micalizio
1Department of Chemistry, The Scripps Research Institute, Jupiter, Florida 33458, USA.
Abstract:
Synthesis of the C1-C26 hexacyclic subunit of pectenotoxin-2 (PTX-2) is described that features a stereoselective annulation to generate the C-ring by triple asymmetric Nozaki-Hiyama-Kishi coupling followed by oxidative cyclization. Preparation of the C1-C14 AB spriroketal-containing subunit employs a recently developed metallacycle-mediated reductive cross-coupling between a TMS-alkyne and a terminal alkene.
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