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- W2078679076 abstract "The total synthesis of the cyclopeptide OF4949-III 1c is described. Key steps are two preparations of didehydroamino acid moieties by condensations of aldehydes and phosphorylglycine esters and two homogeneous hydrogenations with more than 98% ee and de, respectively, to give derivatives of isodityrosine 8a,b. The peptide ring is constructed by the cyclization of an (ω-aminopentafluorophenyl ester in a two phase system in 40% yield." @default.
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- W2078679076 date "1988-01-01" @default.
- W2078679076 modified "2023-10-17" @default.
- W2078679076 title "Total synthesis of of4949-III, a natural inhibitor of aminopeptidase B from ehrlich ascites carcinoma cells" @default.
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- W2078679076 doi "https://doi.org/10.1016/0040-4039(88)85128-1" @default.
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