作者: Du-Bong Choi , Hansol Choi , Jihoon Lee , Yeon-Ju Lee , Hyi-Seung Lee
DOI: 10.1039/D0OB02107E
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摘要: We describe a divergent and enantioselective total synthesis of (+)-ieodomycin A B with three stereoisomers. The main advantage the present is late-stage elaboration side chain, which would afford wide range structurally diverse analogs interesting bioactivities.