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Updated: Apr 23, 2026

Constructing Cyclic Peptides Using an On-Tether Sulfonium Center
Published on: September 28, 2022
Stereoselective total synthesis of marine cyclodepsipeptide calcaripeptides A-C
Sayantan Das1, Rajib Kumar Goswami
1Department of Organic Chemistry, Indian Association for the Cultivation of Science , Jadavpur, Kolkata-700032, India.
Abstract:
The first stereoselective total syntheses of marine cyclodepsipeptides, calcaripeptides A-C, have been accomplished. Emphasis was given particularly in identification of an efficient strategy for the macrocyclization. The notable features of our synthesis include Evans alkylation, Crimmins syn-aldol, Crimmins acetate aldol, Wittig olefination, and Shiina macrolactonization reactions. An anomaly in the (1)H NMR of the proposed calcaripeptide B has been amended during this synthetic study.
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