Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/22132
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dc.contributor.authorHadizadeh, F-
dc.contributor.authorShafiee, A-
dc.contributor.authorKazemi, R-
dc.contributor.authorMohammadi, M-
dc.date.accessioned2013-10-17T06:22:18Z-
dc.date.available2013-10-17T06:22:18Z-
dc.date.issued2002-12-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/22132-
dc.description2679-2682en_US
dc.description.abstracto-Nitrophenyl group of nifedipine has been replaced with 2-alkylthio-1-phenylmethyl-5-im idazolyl substituent. Starting from dihydroxyacetone and phenylmethylamine hydrochloride, 2-alkythio-l-phenylmethyl-5-formylimidazole 3 is first synthesized and subsequently used in synthesizing symmetrical (5a-f) and asymmetrical (6a,b) dihydropyridines.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.41B(12) December 2002]en_US
dc.titleSynthesis of 4-(1-phenylmethyl-5-imidazolyl)-1,4-dihydropyridines as calcium channel antagonistsen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.41B(12) December 2002]

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