Novel syntheses of densely functionalized indolizines, di- and tetrahydroindolizines from 2-formyl-1,4-dihydropyridine systems based on cascade process
Identifieur interne : 001005 ( France/Analysis ); précédent : 001004; suivant : 001006Novel syntheses of densely functionalized indolizines, di- and tetrahydroindolizines from 2-formyl-1,4-dihydropyridine systems based on cascade process
Auteurs : Štefan Marchal N ; Katar Na Cvopová ; Duy-Phong Pham-Huu ; Miloslav Chud K ; Jozef Kozisek ; Ingrid Svoboda [Allemagne] ; Adam Da Ch [France]Source :
- Tetrahedron Letters [ 0040-4039 ] ; 2001.
English descriptors
- KwdEn :
Abstract
Several indolizines, di- and tetrahydroindolizines have been synthesized successfully in a one-pot procedure, in two or three steps from 2-formyl-1,4-dihydropyridine derivatives and malonitrile in 57–87% yield. The general mechanism leading to these azacyclic compounds, involving 2-dicyanovinyl-1,4-dihydropyridines, is discussed.
Url:
DOI: 10.1016/S0040-4039(01)01054-1
Affiliations:
- Allemagne, France
- District de Darmstadt, Haute-Normandie, Hesse (Land), Région Normandie
- Darmstadt, Le Havre
- Université du Havre
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: 000693
- to stream Istex, to step Curation: 000693
- to stream Istex, to step Checkpoint: 000856
- to stream Main, to step Merge: 001819
- to stream Main, to step Curation: 001776
- to stream Main, to step Exploration: 001776
- to stream France, to step Extraction: 001005
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<front><div type="abstract" xml:lang="en">Several indolizines, di- and tetrahydroindolizines have been synthesized successfully in a one-pot procedure, in two or three steps from 2-formyl-1,4-dihydropyridine derivatives and malonitrile in 57–87% yield. The general mechanism leading to these azacyclic compounds, involving 2-dicyanovinyl-1,4-dihydropyridines, is discussed.</div>
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