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-alkylselenodi- and tetrahydropyridine-3-carbonitriles. The structures of the latter products were analyzed by X-ray diffraction.
Authors
- К. А. Фролов (ORCID: https://orcid.org/0000-0002-8045-7582)
- С. Г. Кривоколыско (ORCID: https://orcid.org/0000-0001-9879-9217)
- B. S. Krivokolysko (ORCID: https://orcid.org/0000-0002-3181-7609)
- Nicolai A. Aksenov (ORCID: https://orcid.org/0000-0002-7125-9066)
Institutions
- North-Caucasus Federal University (RU)
- Luhansk State Medical University (UA)
Publication Details
- Journal
- Russian Journal of Organic Chemistry
- Published
- 2025-05-01
- DOI
- https://doi.org/10.1134/s1234567825601111
- Primary Topic
- Organoselenium and organotellurium chemistry
- Type
- article
- Field-Weighted Citation Impact
- 0.00