Results 251 to 260 of about 19,839 (264)
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Enantioselective analysis of 1, 4-dihydropyridine drugs by luquid chromatography
2004The analyses for the following substances were performed: isradipine, nitrendipine, nicardipine, nisoldipine and felodipine. The most successful separations for the all investigated compounds were achieved on Chiralpak AD column that consist of amylose tris(3, 5-dimethylphenylcarbamat) as chiral selector.
Kalčić, Igor +2 more
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Enantioselective and diastereoselective preparation of 1, 4-dihydropyridines
2004Ispitane su različite metode za pripravu enantiomerno čistih 1, 4-dihidropiridinskih spojeva (1, 4-DHP). Rezultati pokazuju da se ovaj tip spojeva dobiva vrlo teško u enantiomerno čistom obliku i da ne postoji jedna općenita metoda za njihovu pripravu.
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Abstract: 1, 4-dihydropyridines and their derivatives are the foremost notable class of Nitrogen-containing heterocyclic scaffolds and have been extensively used since they are occupying the highest position in the pharmaceutical industry because of its wider range of biological and medicinal uses.
Sodah, Karun +2 more
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Sodah, Karun +2 more
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Synthesis and Biological Evaluation of New 1, 4-Dihydropyridines as Antihypertensives Agents in Rats
2003New analogues of nifedipine, as a known calcium channel blocker, were synthesized by replacing the orthonitrophenyl group on position 4 with 1-(4-Nitrobenzyl)-5-imidazolyl or 2methylthio-1-(4-Nitrobenzyl)-5-imidazolyl substituent. Effects of the new synthesized compounds on blood pressure were studied at 15, 30 and 60 min after administration by ...
Jorjani, M +5 more
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Synthese de diacyl-1,4 alcoyl-4 dihydropyridines
Tetrahedron Letters, 1969P.M. Atlani, J.F. Biellmann
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Synthesis and pharmacological activity of 4-aryl-l,4-dihydropyridines
Pharmaceutical Chemistry Journal, 1982V. V. Kastron +9 more
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Rotational Barriers of 4‐Aryl‐1, 4‐dihydropyridines (Ca Antagonists)
Angewandte Chemie International Edition in English, 1984Siegfried Goldmann, Walter Geiger
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2005
In this study we wish to report that t-butyl hydroperoxide is very efficient oxidant in the presence of iron(III)(phthalocyanine)Cl as catalyst for aromatization of 1, 4-DHPs (I), Scheme 1. These reactions are very clean and completed within ca. 30 minutes depending on substituents attached at phenyl ring.
Vinković, Vladimir +2 more
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In this study we wish to report that t-butyl hydroperoxide is very efficient oxidant in the presence of iron(III)(phthalocyanine)Cl as catalyst for aromatization of 1, 4-DHPs (I), Scheme 1. These reactions are very clean and completed within ca. 30 minutes depending on substituents attached at phenyl ring.
Vinković, Vladimir +2 more
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Oxidative and photooxidative phosphorylation by means of 1-phosphoryl-1, 4-dihydropyridines
Tetrahedron Letters, 1973Shozo Matsumoto +3 more
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Synthesis, properties, and cardiovascular activity of substituted 4-dihydropyridine-2(3H)-thiones
Pharmaceutical Chemistry Journal, 1988A. A. Krauze +3 more
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