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- W2109667191 abstract "Rates of bromination at the 5-positions of the title compounds have been measured in aqueous sulfuric acid solutions. The reaction involves a rapid irreversible formation of a 5-bromo-4,6-dihydroxy-hexahydro-2-oxopyrimidine which undergoes slow acid-catalyzed conversion to the corresponding 5-bromopyrimidinone. If excess bromine is present the latter product reacts further to produce a 5,5-dibromo-4,6-dihydroxyhexahydropyrimidine." @default.
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- W2109667191 date "1974-02-01" @default.
- W2109667191 modified "2023-09-23" @default.
- W2109667191 title "The Mechanism of Bromination of 2(1H)-Pyrimidinone, its N-Methyl and N,N′-Dimethyl Derivatives in Aqueous Acidic Solution" @default.
- W2109667191 doi "https://doi.org/10.1139/v74-072" @default.
- W2109667191 hasPublicationYear "1974" @default.
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