Issue 3, 1969

Studies on heterocyclic chemistry. Part II. 4-Alkylidene- and 4-arylidene-isoxazol-5-ones. Participation in and retrogression of the Michael adducts

Abstract

A product C11H14N2O4 obtained in the reaction of ethyl acetoacetate and hydroxylamine has been identified as (II), and evidence is presented that it was formed through 4-isopropylidene-3-methylisoxazol-5-one (III). A Michael reaction of 4-benzylidene-3-methylisoxazol-5-one (VII) is also recorded.

Article information

Article type
Paper

J. Chem. Soc. C, 1969, 363-365

Studies on heterocyclic chemistry. Part II. 4-Alkylidene- and 4-arylidene-isoxazol-5-ones. Participation in and retrogression of the Michael adducts

T. Nishiwaki, J. Chem. Soc. C, 1969, 363 DOI: 10.1039/J39690000363

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