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Updated: Mar 23, 2026

Preparation of Stable Bicyclic Aziridinium Ions and Their Ring-Opening for the Synthesis of Azaheterocycles
Published on: August 22, 2018
Synthesis of the C22-C40 Domain of the Azaspiracids
Zhigao Zhang1, Yong Chen1, Daniel Adu-Ampratwum1
1Department of Chemistry and Biochemistry, The Ohio State University , Columbus, Ohio 43210, United States.
Abstract:
An efficient synthesis of the C22-C40 domain of the azaspiracids is described. The synthetic route features a Nozaki-Hiyama-Kishi (NHK) coupling and chelation controlled Mukaiyama aldol reaction to access an acyclic intermediate and a double-intramolecular-hetero-Michael addition (DIHMA) to provide the FG-ring system bridged ketal.
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