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Title: Total Synthesis of Antibacterial Macrolide Sorangiolide A. Author: Sahana MH, Paul D, Sharma H, Goswami RK. Journal: Org Lett; 2023 Nov 03; 25(43):7827-7831. PubMed ID: 37856450. Abstract: A convergent route for the asymmetric total synthesis of antibacterial macrolide sorangiolide A has been developed for the first time. The key feature of this synthesis includes Krische iridium-catalyzed anti-diastereoselective carbonyl crotylation, Crimmins acetate aldol, Yamaguchi esterification, Julia-Kocienski olefination, Horner-Wadsworth-Emmons olefination, and ring-closing metathesis. The origin of the low intensity of the 13C{1H} NMR signals of the C1 and C2 centers of the natural product has been investigated, disclosing possible forms of existence for the natural product in the solution phase.[Abstract] [Full Text] [Related] [New Search]