Synthesis of new tetrahydropyrido[1,2-a]benzimidazoles based on recyclization of N-arylitaconimides with 2-cyanomethylbenzimidazole Full article
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Mendeleev Communications
ISSN: 1364-551X , E-ISSN: 0959-9436 |
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| Output data | Year: 2021, Volume: 31, Number: 2, Pages: 254-256 Pages count : 3 DOI: 10.1016/j.mencom.2021.03.037 | ||||
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Abstract:
A convenient preparative synthesis of N-aryl-2-(4-cyano-3-oxo-1,2,3,5-tetrahydropyrido[1,2-a]benzimidazol-2-yl)acetamides is based on the reflux of N-arylitaconimides with 2-cyanomethylbenzimidazole in acetic acid.
Cite:
Shmoylova Y.Y.
, Kovygin Y.A.
, Ledenyova I.V.
, Prezent M.A.
, Baranin S.V.
, Shikhaliev K.S.
Synthesis of new tetrahydropyrido[1,2-a]benzimidazoles based on recyclization of N-arylitaconimides with 2-cyanomethylbenzimidazole
Mendeleev Communications. 2021. V.31. N2. P.254-256. DOI: 10.1016/j.mencom.2021.03.037 WOS Scopus OpenAlex
Synthesis of new tetrahydropyrido[1,2-a]benzimidazoles based on recyclization of N-arylitaconimides with 2-cyanomethylbenzimidazole
Mendeleev Communications. 2021. V.31. N2. P.254-256. DOI: 10.1016/j.mencom.2021.03.037 WOS Scopus OpenAlex
Identifiers:
| ≡ Web of science: | WOS:000635839800037 |
| ≡ Scopus: | 2-s2.0-85105008497 |
| ≡ OpenAlex: | W3144659209 |