The stereochemistry of the β-hydroxyleucine unit of frangulanine

Abstract
1 H n.m.r. spectral analysis shows that the β-hydroxyleucine portion of the peptide alkaloids frangulanine and discarine A and B possess and erythro-configuration; stereochemical analysis of frangulanine by enzymic oxidation of its product of reduction and subsequent hydrolysis reveals the subunit to be of the L-erythro-β-hydroxyleucine-type.

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