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
β¦ LIBER β¦
Acetylation of the thallium(I) salt of 2(1H)-pyridone. Formation of N-acetyl-2-(1H)-pyridone.
β Scribed by Alexander Mckillop; Michael J. Zelesko; Edward C. Taylor
- Publisher
- Elsevier Science
- Year
- 1968
- Tongue
- French
- Weight
- 215 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0040-4039
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