Abstract
Literature and characteristic experimental data correlated in the review concern the intramolecular cyclization by various means of substituted 1,5-diketones of the acyclic, semi-, and bicyclic series, proceeding to the formation of oxygen-containing heterocycles, such as pyrans, pyrylium salts, di- and tetrahydrofurans, and their condensed analogs, aroylfurans etc.
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Kharchenko, V.G., Pchelintseva, N.V., Markova, L.I. et al. Oxygen-containing Heterocyclic Compounds from 1,5-Diketones. (Review). Chemistry of Heterocyclic Compounds 36, 1007–1025 (2000). https://doi.org/10.1023/A:1002730329179
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DOI: https://doi.org/10.1023/A:1002730329179
- synthesis
- structure
- properties
- 1,5-diketones
- pentane-1,5-diones
- 2-pentene-1,5-diones
- 1,3,5-triaryl-2,4-dichloro-2-pentene-1,5-diones
- arylidenedicyclanones
- heterylidenedicyclanones
- 2-(3-oxo-1,3-diphenylpropyl)tetralones
- 4-(1,3-diaryl-3-oxopropyl)pyrazolones
- pyrans
- dihydropyrans
- tetrahydropyrans
- sym-octahydroxanthenes
- pyrylium salts
- aroylfurans
- 2-aroyl-4-chlorofurans