Issue 16, 1982

Partial synthesis of 11-oxygenated erythrina alkaloids

Abstract

Lead tetra-acetate oxidation of erysovine (7) afforded 11α-acetoxyerysovine (8) whereas the isomer, erysodine (6) afforded a quinone derivative (10), which was subsequently transformed into an 11 β-acetoxyerysodine derivative (15), and the aromatic oxidation products (11a) and (11b).

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1982, 904-905

Partial synthesis of 11-oxygenated erythrina alkaloids

Maysoon. I. Abdullah, A. S. Chawla and Anthony. H. Jackson, J. Chem. Soc., Chem. Commun., 1982, 904 DOI: 10.1039/C39820000904

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