SYNTHESIS OF N-SUBSTITUTED 3-HYDROXY-2-METHYL-4-PYRIDONES AND 3-HYDROXY-2-METHYL-4-PYRIDONIMINES

Citation
M. Farber et al., SYNTHESIS OF N-SUBSTITUTED 3-HYDROXY-2-METHYL-4-PYRIDONES AND 3-HYDROXY-2-METHYL-4-PYRIDONIMINES, Journal of heterocyclic chemistry, 31(4), 1994, pp. 947-956
Citations number
24
Categorie Soggetti
Chemistry Inorganic & Nuclear
ISSN journal
0022152X
Volume
31
Issue
4
Year of publication
1994
Pages
947 - 956
Database
ISI
SICI code
0022-152X(1994)31:4<947:SON3A3>2.0.ZU;2-R
Abstract
Carbohydrates with 1,4 glycosidic bonds like maltose, lactose, dextrin or starch react with primary amines as well as amino acids or protein s to give i.e. 3-hydroxy-2-methyl-4-pyridones 5 and 3-hydroxy-2-methyl -4-pyridonimines 7. A generally applicable synthesis of compounds of t his type is described. The pyridones S and pyridonimines 7 are strongl y complexing agents. Molybdenum-derivatives, for instance, are suitabl e as fairly stable oxidation catalysts.