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Mass spectral fragmentation patterns of new 5-acetyl-4-aryl-6-methyl-2(1H)pyridones

โœ Scribed by Roberto Martinez; Margarita Suarez; Nazario Martin; Estael Ochoa; Carlos Seoane; Yamila Verdecia


Publisher
John Wiley and Sons
Year
1999
Tongue
English
Weight
36 KB
Volume
13
Category
Article
ISSN
0951-4198

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โœฆ Synopsis


The electron impact mass spectra of new 5-acetyl-4-aryl-6-methyl-2(1H)pyridones have been studied. A dominant peak in all the spectra is due to cleavage of the CO-NH bond of the amido group with charge retention on the carbonyl group. This fragmentation is followed by a hydrogen rearrangement to the nitrogen atom forming ketene intermediates; this pathway leads to a highly stabilized ion which constitutes the base peak in the spectra in most of the compounds studied.


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