1417908-53-2Relevant academic research and scientific papers
Formal total synthesis of (-)-5,6-dihydrocineromycine B
Reddy, G. Venkateswar,Kumar, R. Sateesh Chandra,Siva,Babu, K. Suresh,Rao, J. Madhusudana
, p. 2677 - 2681 (2012)
An efficient and highly convergent formal total synthesis of the 14-membered macrolide (-)-5,6-dihydrocineromycine B is achieved. Key reaction sequences include a Sharpless asymmetric epoxidation followed by esterification for the formation of a fully functionalized acyclic precursor, Corey-Bakshi-Shibata reduction, and ring-closing metathesis, respectively. Georg Thieme Verlag KG Stuttgart · New York.
