Issue 8, 1988

Absolute stereochemistry of proclavaminic acid, the monocyclic biosynthetic precursor of clavulanic acid

Abstract

Proclavaminic acid (1) has been synthesized by a route which indicated the absolute stereochemistry of the two chiral centres to be (2S,3R).

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1988, 567-568

Absolute stereochemistry of proclavaminic acid, the monocyclic biosynthetic precursor of clavulanic acid

K. H. Baggaley, N. H. Nicholson and J. T. Sime, J. Chem. Soc., Chem. Commun., 1988, 567 DOI: 10.1039/C39880000567

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