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- W2084428343 endingPage "1934" @default.
- W2084428343 startingPage "1925" @default.
- W2084428343 abstract "Acylation of 5,5-diphenylimidazolid-4-one gives 1,3-diacyl-5,5-diphenylimidazolid-4-ones, and not 2-acyl-4,4-diphenyl-2,5-diaza-7-oxabicyclo[3.2.0]heptan-3-ones as claimed by Biltz and his co-workers. The reason for the unusual stability of the N 1 -acyl groups to acid and alkaline hydrolysis is discussed. The revised formulation allows the oxidation products of 1-acetyl-5,5-diphenylimidazolid-4-one to be rationalized in a simple fashion." @default.
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- W2084428343 date "1967-09-01" @default.
- W2084428343 modified "2023-10-16" @default.
- W2084428343 title "Acylation products of 5,5-diphenylimidazolid-4-one" @default.
- W2084428343 doi "https://doi.org/10.1139/v67-308" @default.
- W2084428343 hasPublicationYear "1967" @default.
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