Abstract
Published data and the authors' own experimental results on the reaction of aliphatic, semicyclic, and oxosemicyclic 1,5-diketones and alkylidene- and arylidene-2,2-dicyclanones with ammonia, ammonium acetate, and XNH2 derivatives, where X = Alk, Ar, OH, NH2, PhNH, ArCONH, and CHO, are reviewed. The characteristics and the relationships governing the transformations into azaheterocycles in relation to the nature of the reagents and the reaction conditions are discussed.
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Kharchenko, V.G., Markova, L.I., Fedotova, O.V. et al. Reactions of 1,5-Diketones with Ammonia and Its Derivatives. (Review). Chemistry of Heterocyclic Compounds 39, 1121–1142 (2003). https://doi.org/10.1023/B:COHC.0000008257.42400.9e
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DOI: https://doi.org/10.1023/B:COHC.0000008257.42400.9e
- alkylidenedicyclanones
- arylidenedicyclanones
- aroylpyrroles
- 3-hydroquinol-2-ones
- dihydro-1,2-diazepines
- N-R-dihydropyridines
- dihydropyridines
- tetrahydropyridines
- 1,5-diketones
- octahydroacridines
- pentane-1,5-diones
- 2-pentene-1,5-diones
- pyrazolines
- pyrazoles
- pyridines
- pyridine bases
- piperidine bases
- semicyclic
- oxosemicyclic 1,5-diketones
- pyridinium salts
- tetrahydroquinolines
- azaheterocyclization
- indolization
- pyridinization
- properties
- synthesis
- structure