Novel synthese of heterocycles with N-(1-haloalkyl)azinium halides. Part 5. Preparation of N-substituted 1,4-dihydropyridines

Article abstract of DOI:10.1080/00397919208021145

Thirty N-substituted Hantzsch 1,4-dihydropyridines were prepared under mild and neutral conditions from N-substituted enaminocarbonyl derivatives and aldehydes activated under the form of N-(1-chloroalkyl)pyridinium chlorides by means of thionyl chloride

Full text of DOI:10.1080/00397919208021145

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Novel Syntheses of
Heterocycles with N-(1-
Haloalkyl)azinium Halides. Part
V. Preparation of N-Substituted
1,4-Dihydropyridines
Jean-Jacques Vanden Eynde a , Annie Mayence a ,
André Maquestiau a & Ernst Anders b
a University of Mons-Hainaut, Organic Chemistry
Laboratory Place du Parc 20, B-7000, Mons, Belgium
b Institut für Organische Chemie der Universität
Erlangen-Nürnberg Henkestr, 42, D-8520, Erlangen,
Germany
Published online: 23 Sep 2006.
To cite this article: Jean-Jacques Vanden Eynde , Annie Mayence , André Maquestiau
& Ernst Anders (1992): Novel Syntheses of Heterocycles with N-(1-Haloalkyl)azinium
Halides. Part V. Preparation of N-Substituted 1,4-Dihydropyridines, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 22:22, 3291-3304
To link to this article: http://dx.doi.org/10.1080/00397919208021145
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