An efficient synthesis of new polyfunctional hexahydro pyrido[1,2-a]pyrazin-1-ones 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: 259-261 Pages count : 3 DOI: 10.1016/j.mencom.2021.03.039 | ||||
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Abstract:
New polyfunctional hydrogenated pyrido[1,2-a]pyrazin- 1-ones were obtained by regioselective recyclization of N-arylitaconimides with alkyl (3-oxopiperazin-2-ylidene)acetates. The supposed cascade reaction pathway involves the Michael addition of the nucleophile to an activated double bond and subsequent intramolecular transamidation of the intermediate with simultaneous recycling.
Cite:
Shmoylova Y.Y.
, Kovygin Y.A.
, Ledenyova I.V.
, Prezent M.A.
, Daeva E.D.
, Baranin S.V.
, Shikhaliev K.S.
An efficient synthesis of new polyfunctional hexahydro pyrido[1,2-a]pyrazin-1-ones
Mendeleev Communications. 2021. V.31. N2. P.259-261. DOI: 10.1016/j.mencom.2021.03.039 WOS Scopus OpenAlex
An efficient synthesis of new polyfunctional hexahydro pyrido[1,2-a]pyrazin-1-ones
Mendeleev Communications. 2021. V.31. N2. P.259-261. DOI: 10.1016/j.mencom.2021.03.039 WOS Scopus OpenAlex
Identifiers:
| ≡ Web of science: | WOS:000635839800039 |
| ≡ Scopus: | 2-s2.0-85104987614 |
| ≡ OpenAlex: | W3145598085 |