Total Synthesis of Olenamidonin B
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Updated: Nov 7, 2026

Preparation of Enantiopure Non-Activated Aziridines and Synthesis of Biemamide B, D, and epiallo-Isomuscarine
Published on: June 13, 2022
Victor R Charette1, Jeremy Goodyear1, Scott D Taylor1
1Department of Chemistry, University of Waterloo, 200 University Avenue West, Waterloo, OntarioN2L 3G1, Canada.
Abstract:
Olenamidonin B is a cyclic lipopeptide antibiotic recently isolated from Streptomyces olivaceus. It exhibits antibacterial activity against Gram-positive bacteria and is especially potent against multidrug-resistant Enterococci. Its unusual bicyclic architecture, featuring a four-amino-acid macrocycle, an imidazolidinone ring, and a rare exocyclic (E)-dehydro-β-alanine-containing fatty acid, presents a compelling synthetic target. Here, we describe the total synthesis of olenimidonin B.
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