Issue 6, 1998

Enantiospecific Synthesis of Analogues of the Diketide Intermediate of the Erythromycin Polyketide Synthase (PKS)

Abstract

The four stereoisomers of 3-hydroxy-2-methylpentanoic acid (1ad) and the structurally modified acids 1ej have been synthesised enantiospecifically and converted into p-nitrophenyl ester and thioester derivatives; as the activated derivatives; they are available for investigations into the substrate selectivity of polyketide synthase (PKS) domains.

Article information

Article type
Paper

J. Chem. Res. (S), 1998, 283-283

Enantiospecific Synthesis of Analogues of the Diketide Intermediate of the Erythromycin Polyketide Synthase (PKS)

R. C. Harris, A. L. Cutter, K. J. Weissman, U. Hanefeld, M. C. Timoney and J. Staunton, J. Chem. Res. (S), 1998, 283 DOI: 10.1039/A800584B

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