Synthesis of 1,4-Dihydropyridines Bearing a Carbamate Moiety on the 4-Position
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. Whe...
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| Format: | Article |
| Language: | English |
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Wiley
2013-01-01
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| Series: | Journal of Chemistry |
| Online Access: | http://dx.doi.org/10.1155/2013/495982 |
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| author | Davood Habibi Mohammad Ali Zolfigol Maliheh Safaee |
| author_facet | Davood Habibi Mohammad Ali Zolfigol Maliheh Safaee |
| author_sort | Davood Habibi |
| collection | DOAJ |
| description | 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. |
| format | Article |
| id | doaj-art-e10e7f4a853c4828bbc2c8c1fc9d4cf4 |
| institution | OA Journals |
| issn | 2090-9063 2090-9071 |
| language | English |
| publishDate | 2013-01-01 |
| publisher | Wiley |
| record_format | Article |
| series | Journal of Chemistry |
| spelling | doaj-art-e10e7f4a853c4828bbc2c8c1fc9d4cf42025-08-20T02:21:29ZengWileyJournal of Chemistry2090-90632090-90712013-01-01201310.1155/2013/495982495982Synthesis of 1,4-Dihydropyridines Bearing a Carbamate Moiety on the 4-PositionDavood Habibi0Mohammad Ali Zolfigol1Maliheh Safaee2Department of Organic Chemistry, Faculty of Chemistry, Bu-Ali Sina University, Hamedan 6517838683, IranDepartment of Organic Chemistry, Faculty of Chemistry, Bu-Ali Sina University, Hamedan 6517838683, IranDepartment of Organic Chemistry, Faculty of Chemistry, Bu-Ali Sina University, Hamedan 6517838683, IranA 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.http://dx.doi.org/10.1155/2013/495982 |
| spellingShingle | Davood Habibi Mohammad Ali Zolfigol Maliheh Safaee Synthesis of 1,4-Dihydropyridines Bearing a Carbamate Moiety on the 4-Position Journal of Chemistry |
| title | Synthesis of 1,4-Dihydropyridines Bearing a Carbamate Moiety on the 4-Position |
| title_full | Synthesis of 1,4-Dihydropyridines Bearing a Carbamate Moiety on the 4-Position |
| title_fullStr | Synthesis of 1,4-Dihydropyridines Bearing a Carbamate Moiety on the 4-Position |
| title_full_unstemmed | Synthesis of 1,4-Dihydropyridines Bearing a Carbamate Moiety on the 4-Position |
| title_short | Synthesis of 1,4-Dihydropyridines Bearing a Carbamate Moiety on the 4-Position |
| title_sort | synthesis of 1 4 dihydropyridines bearing a carbamate moiety on the 4 position |
| url | http://dx.doi.org/10.1155/2013/495982 |
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