Unusual transformation of substituted-3-formylchromones to pyrimidine analogues: Synthesis and antimicrobial activities of 5-(o-hydroxyaroyl) pyrimidines

Bioorganic and Medicinal Chemistry Letters

Volumn 23, Issue 22, 2013, Pages 6093-6096

  Raj, Tilak ^a   Singh, Narinder ^a   Ishar, M P S ^b  

^a INDIAN INSTITUTE OF TECHNOLOGY ROPAR   (India)

^b GURU NANAK DEV UNIVERSITY   (India)

Author keywords

3 Formylchromones; Antibacterial activities; Antifungal activities; Azadienes; Pyrimidines

Indexed keywords

1,3 BIS DIMETHYLAMINOMETHYLENE THIOUREA; 5 (O HYDROXYAROYL)PYRIMIDINE; CHROMONE DERIVATIVE; CIPROFLOXACIN; FLUCONAZOLE; PYRIMIDINE DERIVATIVE; THIOUREA; TOLUENE; UNCLASSIFIED DRUG;

ANTIFUNGAL ACTIVITY; ANTIMICROBIAL ACTIVITY; ARTICLE; BACTERIAL GROWTH; BACTERIAL STRAIN; CANDIDA TROPICALIS; CONTROLLED STUDY; DRUG CYTOTOXICITY; DRUG STRUCTURE; DRUG SYNTHESIS; ESCHERICHIA COLI; FUNGAL STRAIN; GALACTOMYCES GEOTRICHUM; GROWTH INHIBITION; IN VITRO STUDY; MINIMUM INHIBITORY CONCENTRATION; PSEUDOMONAS AERUGINOSA; SHIGELLA FLEXNERI; STAPHYLOCOCCUS AUREUS;

BACTERIA (MICROORGANISMS); GALACTOMYCES GEOTRICHUM;

3-FORMYLCHROMONES; ANTIBACTERIAL ACTIVITIES; ANTIFUNGAL ACTIVITIES; AZADIENES; PYRIMIDINES;

ANTI-BACTERIAL AGENTS; ANTIFUNGAL AGENTS; CANDIDA; CHROMONES; GEOTRICHUM; HELA CELLS; HUMANS; MICROBIAL SENSITIVITY TESTS; PYRIMIDINES; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 84885950703     PISSN: 0960894X     EISSN: 14643405     Source Type: Journal    
DOI: 10.1016/j.bmcl.2013.09.024     Document Type: Article

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