Stereoselective total synthesis of Aspergillide D.
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DOI: 10.1080/14786419.2022.2078321
Abstract: The total synthesis of the 16-membered Polyhydroxylated macrolide, Aspergillide D has been accomplished utilizing the Grignard reaction, Sharpless asymmetric epoxidation Regioselective ring opening of epoxy alcohol, Wittig olefination and Yamaguchi macrolactonisation as key steps. 3-butene-1-ol… read more here.
Keywords: total synthesis; synthesis aspergillide; stereoselective total; synthesis ... See more keywords