Affiliation:
1. Institut für Organische Chemie und Biochemie der Universität Freiburg, Albertstraße 21, D-7800 Freiburg
Abstract
Abstract
Mono-and diquaternary pyridinium salts substituted in 3-position with electron with-drawing groups, react with alcohols under basic conditions to give 6-alcoxy-1,6-dihydro-pyridines. Symmetric dipyridinium salts react in aqueous alkaline solution to products with 6-pyridone and dihydropyridine moiety. This redox reaction depends on the length of the bridge connecting the pyridinium rings. Pyridinium salts can be reduced by aluminiumtriisopropoxide to 1,4-dihydropyridines.
Cited by
10 articles.
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