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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Pleiades Publishing
2025
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ir-123456789-318432025-08-12T11:57:41Z Dibenzoylmethane in the Synthesis of Selenium Di- and Tetrahydropyridine-3-carbonitriles Aksenov, N. A. Аксенов, Н. А. 1,4,5,6-tetrahydropyridine 1,4-dihydropyridine 2-furancarbaldehyde 2-thiophencarbaldehyde Cyanoselenoacetamide Dibenzoylmethane Ethyl Chloroacetate Methyl Iodide 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. 2025-08-12T11:56:53Z 2025-08-12T11:56:53Z 2025 Статья Frolov, K. A., Krivokolysko, B. S., Aksenov, N. A., Krivokolysko, S. G. Dibenzoylmethane in the Synthesis of Selenium Di- and Tetrahydropyridine-3-carbonitriles // Russian Journal of Organic Chemistry. - 2025. - 61 (5). - pp. 826 - 830. - DOI: 10.1134/S1234567825601111 https://dspace.ncfu.ru/handle/123456789/31843 ru Russian Journal of Inorganic Chemistry application/pdf application/pdf Pleiades Publishing |
| institution |
СКФУ |
| collection |
Репозиторий |
| language |
Russian |
| topic |
1,4,5,6-tetrahydropyridine 1,4-dihydropyridine 2-furancarbaldehyde 2-thiophencarbaldehyde Cyanoselenoacetamide Dibenzoylmethane Ethyl Chloroacetate Methyl Iodide |
| spellingShingle |
1,4,5,6-tetrahydropyridine 1,4-dihydropyridine 2-furancarbaldehyde 2-thiophencarbaldehyde Cyanoselenoacetamide Dibenzoylmethane Ethyl Chloroacetate Methyl Iodide Aksenov, N. A. Аксенов, Н. А. Dibenzoylmethane in the Synthesis of Selenium Di- and Tetrahydropyridine-3-carbonitriles |
| description |
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. |
| format |
Статья |
| author |
Aksenov, N. A. Аксенов, Н. А. |
| author_facet |
Aksenov, N. A. Аксенов, Н. А. |
| author_sort |
Aksenov, N. A. |
| title |
Dibenzoylmethane in the Synthesis of Selenium Di- and Tetrahydropyridine-3-carbonitriles |
| title_short |
Dibenzoylmethane in the Synthesis of Selenium Di- and Tetrahydropyridine-3-carbonitriles |
| title_full |
Dibenzoylmethane in the Synthesis of Selenium Di- and Tetrahydropyridine-3-carbonitriles |
| title_fullStr |
Dibenzoylmethane in the Synthesis of Selenium Di- and Tetrahydropyridine-3-carbonitriles |
| title_full_unstemmed |
Dibenzoylmethane in the Synthesis of Selenium Di- and Tetrahydropyridine-3-carbonitriles |
| title_sort |
dibenzoylmethane in the synthesis of selenium di- and tetrahydropyridine-3-carbonitriles |
| publisher |
Pleiades Publishing |
| publishDate |
2025 |
| url |
https://dspace.ncfu.ru/handle/123456789/31843 |
| work_keys_str_mv |
AT aksenovna dibenzoylmethaneinthesynthesisofseleniumdiandtetrahydropyridine3carbonitriles AT aksenovna dibenzoylmethaneinthesynthesisofseleniumdiandtetrahydropyridine3carbonitriles |
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