Issue 15, 1994

Photolysis of phenyldisic acids: evidence for unique product formation from discrete tautomers

Abstract

3-Hydroxy-2-methyl-4-phenylisoxazol-5(2H)-one exists as four tautomers, two of which are isolated and characterised; photolysis in methanol leads to formation of products identified as arising uniquely from three of the tautomers, and the 2-phenyl analogue and phenyldisic acid undergo similar photochemical reactions.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1994, 1805-1806

Photolysis of phenyldisic acids: evidence for unique product formation from discrete tautomers

R. H. Prager and J. A. Smith, J. Chem. Soc., Chem. Commun., 1994, 1805 DOI: 10.1039/C39940001805

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