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Volumn 47, Issue 1, 2012, Pages 18-23
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Efficient one-pot preparation of novel fused chromeno[2,3-d]pyrimidine and pyrano[2,3-d]pyrimidine derivatives
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Author keywords
Antibacterial activity; Antifungal activity; Pyrimidine
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Indexed keywords
5 (ETHOXYMETHYLENE) 2 THIOXO DIHYDROPYRIMIDINE 4,6 (1H,5H)DIONE;
5 (HYDRAZINYLMETHYLENE) 2 THIOXO DIHYDROPYRIMIDINE 4,6 (1H,5H)DIONE;
6,8 DIAMINO 4 OXO 2 THIOXO 5 (3,4,5 TRIMETHOXYPHENYL) 2,3,4,5 TETRAHYDRO 1H PYRIDO[3',2' 4,5]PYRANO[2,3 DEXTRO]PYRIMIDINE 7 CARBONITRILE;
7 AMINO 4 OXO 2 THIOXO 5 (3,4,5 TRIMETHOXYPHENYL) 2,3,4,5 TETRAHYDRO 1H PYRANO[2,3 DEXTRO]PYRIMIDINE 6 CARBONITRILE;
8 HYDROXY 2 THIOXO 2,3 DIHYDROCHROMENO[2,3 DEXTRO]PYRIMIDIN 4 ONE;
AMPHOTERICIN;
ETHYL 7 AMINO 5 (4 CHLOROPHENYL) 2,4 DITHIOXO 2,3,4,5 TETRAHYDRO 1H THIOPYRANO[2,3 D]PYRIMIDINE 6 CARBOXYLATE;
ETHYL 7 AMINO 5 (4 CHLOROPHENYL) 4 OXO 2 THIOXO 2,3,4,5 TETRAHYDRO 1H PYRANO[2,3 DEXTRO]PYRIMIDINE 6 CARBOXYLATE;
N (6 CYANO 4 OXO 2 THIOXO 5 (3,4,5 TRIMETHOXYPHENYL) 2,3,4,5 TETRAHYDRO 1H PYRANO[2,3 D]PYRIMIDIN 7 YL)BENZENESULFONAMIDE;
PYRIMIDINE DERIVATIVE;
TETRACYCLINE;
UNCLASSIFIED DRUG;
ANTIFUNGAL ACTIVITY;
ANTIMICROBIAL ACTIVITY;
ARTICLE;
ASPERGILLUS FLAVUS;
CANDIDA ALBICANS;
CHEMICAL REACTION;
CONTROLLED STUDY;
DRUG EFFICACY;
DRUG STRUCTURE;
DRUG SYNTHESIS;
MINIMUM INHIBITORY CONCENTRATION;
NONHUMAN;
ONE POT SYNTHESIS;
PSEUDOMONAS AERUGINOSA;
SPECTROSCOPY;
STAPHYLOCOCCUS AUREUS;
ANTI-INFECTIVE AGENTS;
ASPERGILLUS FLAVUS;
BENZOPYRANS;
CANDIDA ALBICANS;
CHEMISTRY TECHNIQUES, SYNTHETIC;
PSEUDOMONAS AERUGINOSA;
PYRANS;
PYRIMIDINES;
STAPHYLOCOCCUS AUREUS;
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EID: 84855762778
PISSN: 02235234
EISSN: 17683254
Source Type: Journal
DOI: 10.1016/j.ejmech.2011.09.040 Document Type: Article |
Times cited : (88)
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References (23)
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