Asymmetric total synthesis of (+)-phoslactomycin B
Setsuya Shibahara1, Masataka Fujino, Yasumasa Tashiro
1Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki, Japan.
Abstract:
(+)-Phoslactomycin B was synthesized by a highly enantio- and stereoselective approach involving asymmetric pentenylation, Suzuki-Miyaura coupling, ring-closing metathesis, asymmetric dihydroxylation, and Stille coupling. The synthetic method developed enables us to synthesize three other isomers concerning the C11-OH and Delta12-double bond.
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