Dibenzoylmethane in the Synthesis of Selenium Di- and Tetrahydropyridine-3-carbonitriles
3-Cyano-6-hydroxy-1,4,5,6-tetrahydropyridine-2-ammonium selenolates have been synthesized by the reaction of cyanoselenoacetamide, furan-2- or thiophene-2-carbaldehyde, and dibenzoylmethane in ethanol in the presence of an excess of piperidine or morpholine under argon and then used to obtain 2-alky...
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| Autores principales: | , |
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| Formato: | Статья |
| Lenguaje: | Russian |
| Publicado: |
Pleiades Publishing
2025
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| Materias: | |
| Acceso en línea: | https://dspace.ncfu.ru/handle/123456789/31843 |
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| Sumario: | 3-Cyano-6-hydroxy-1,4,5,6-tetrahydropyridine-2-ammonium selenolates have been synthesized by the reaction of cyanoselenoacetamide, furan-2- or thiophene-2-carbaldehyde, and dibenzoylmethane in ethanol in the presence of an excess of piperidine or morpholine under argon and then used to obtain 2-alkylselenodi- and tetrahydropyridine-3-carbonitriles. The structures of the latter products were analyzed by X-ray diffraction. |
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