Issue 7, 1999

Regioselective Addition of Grignard Reagents to Isoxazole-4,5-dicarboxylate Esters

Abstract

Regioselective mono-addition of a range of Grignard reagents with the 5-esters of 3-methylisoxazole-4,5-diesters affords 5-keto derivatives instead of tertiary alcohols which is explained by the complexing ability of the isoxazole oxygen atom and by the electron withdrawing effect of the isoxazole ring.

Article information

Article type
Paper

J. Chem. Res. (S), 1999, 428-429

Regioselective Addition of Grignard Reagents to Isoxazole-4,5-dicarboxylate Esters

K. J. Batchelor, W. Russell Bowman, R. V. Davies, M. H. Hockley and D. J. Wilkins, J. Chem. Res. (S), 1999, 428 DOI: 10.1039/A902259G

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