![](/images/graphics-bg.png)
Synthesis of 1,4-Dihydropyridines Bearing a Carbamate Moiety on the 4-Position
Joint Authors
Safaee, Maliheh
Habibi, Dawud
Zolfigol, Mohammad Ali
Source
Issue
Vol. 2013, Issue 2013 (31 Dec. 2013), pp.1-6, 6 p.
Publisher
Hindawi Publishing Corporation
Publication Date
2013-07-28
Country of Publication
Egypt
No. of Pages
6
Main Subjects
Abstract EN
A good range of 1,4-dihydropyridines bearing a carbamate moiety on the 4-position were synthesized from the primary reaction of different hydroxyaldehydes with phenyl isocyanates and the subsequent reaction of the obtained carbamates with methyl acetoacetate in the presence of ammonium fluoride.
When phenyl isothiocyanate was used in place of phenyl isocyanate in the same condition, the reaction did not take place.
American Psychological Association (APA)
Habibi, Dawud& Zolfigol, Mohammad Ali& Safaee, Maliheh. 2013. Synthesis of 1,4-Dihydropyridines Bearing a Carbamate Moiety on the 4-Position. Journal of Chemistry،Vol. 2013, no. 2013, pp.1-6.
https://search.emarefa.net/detail/BIM-476273
Modern Language Association (MLA)
Habibi, Dawud…[et al.]. Synthesis of 1,4-Dihydropyridines Bearing a Carbamate Moiety on the 4-Position. Journal of Chemistry No. 2013 (2013), pp.1-6.
https://search.emarefa.net/detail/BIM-476273
American Medical Association (AMA)
Habibi, Dawud& Zolfigol, Mohammad Ali& Safaee, Maliheh. Synthesis of 1,4-Dihydropyridines Bearing a Carbamate Moiety on the 4-Position. Journal of Chemistry. 2013. Vol. 2013, no. 2013, pp.1-6.
https://search.emarefa.net/detail/BIM-476273
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references
Record ID
BIM-476273