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Volumn 45, Issue 12, 2010, Pages 5848-5855
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Post Groebke-Blackburn multicomponent protocol: Synthesis of new polyfunctional imidazo[1,2-a]pyridine and imidazo[1,2-a]pyrimidine derivatives as potential antimicrobial agents
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Author keywords
Antibacterial agents; Benzimidazole; Imidazopyridine; Imidazopyrimidine; Oxadiazole; Phenyl imidazole
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Indexed keywords
2 (4 BROMOPHENYL) 6 (6 CHLORO 1H BENZO[D]IMIDAZOL 2 YL) N PHENYLIMIDAZO[1,2 A]PYRIMIDIN 3 AMINE;
2 (4 BROMOPHENYL) 6 (6 FLUORO 1H BENZO[D]IMIDAZOL 2 YL) N PHENYLIMIDAZO[1,2 A]PYRIDIN 3 AMINE;
2 (4 BROMOPHENYL) 6 (6 FLUORO 1H BENZO[D]IMIDAZOL 2 YL) N PHENYLIMIDAZO[1,2 A]PYRIMIDIN 3 AMINE;
2 (4 BROMOPHENYL) 6 (6 METHYL 1H BENZO[D]IMIDAZOL 2 YL) N PHENYLIMIDAZO[1,2 A]PYRIDIN 3 AMINE;
2 (4 BROMOPHENYL) 6 (6 NITRO 1H BENZO[D]IMIDAZOL 2 YL) N PHENYLIMIDAZO[1,2 A]PYRIDIN 3 AMINE;
2 (4 BROMOPHENYL) 6 (6 NITRO 1H BENZO[D]IMIDAZOL 2 YL) N PHENYLIMIDAZO[1,2 A]PYRIMIDIN 3 AMINE;
2 (4 BROMOPHENYL) 6 (6 PHENOXY 1H BENZO[D]IMIDAZOL 2 YL) N PHENYLIMIDAZO[1,2 A]PYRIDIN 3 AMINE;
2 (4 BROMOPHENYL) 6 [5 (4 CHLOROPHENYL) 1H BENZO[D]IMIDAZOL 2 YL] N PHENYLIMIDAZO[1,2 A]PYRIDIN 3 AMINE;
2 (4 BROMOPHENYL) 6 [5 (4 CHLOROPHENYL) 1H IMIDAZOL 2 YL] N PHENYLIMIDAZO[1,2 A]PYRIMIDIN 3 AMINE;
2 (4 BROMOPHENYL) 6 [5 (4 FLUOROPHENYL) 1,3,4 OXADIAZOL 2 YL] N PHENYLIMIDAZO[1,2 A]PYRIDIN 3 AMINE;
2 (4 BROMOPHENYL) 6 [5 (4 FLUOROPHENYL) 1H BENZO[D]IMIDAZOL 2 YL] N PHENYLIMIDAZO[1,2 A]PYRIDIN 3 AMINE;
2 (4 BROMOPHENYL) 6 [5 (4 FLUOROPHENYL) 1H IMIDAZOL 2 YL] N PHENYLIMIDAZO[1,2 A]PYRIMIDIN 3 AMINE;
2 (4 BROMOPHENYL) 6 [5 (4 NITROPHENYL) 1,3,4 OXADIAZOL 2 YL] N PHENYLIMIDAZO[1,2 A]PYRIDIN 3 AMINE;
2 (4 BROMOPHENYL) 6 [5 (4 PHENOXYPHENYL) 1H BENZO[D]IMIDAZOL 2 YL] N PHENYLIMIDAZO[1,2 A]PYRIDIN 3 AMINE;
2 (4 BROMOPHENYL) N PHENYL 6 [5 (4 TOLYL) 1,3,4 OXADIAZOL 2 YL]IMIDAZO[1,2 A]PYRIDIN 3 AMINE;
6 (6 BROMO 1H BENZO[D]IMIDAZOL 2 YL) N PHENYL 2 (4 TOLYLIMIDAZO[1,2 A]PYRIDIN) 3 AMINE;
6 (6 FLUORO 1H BENZO[D]IMIDAZOL 2 YL) 2 (4 PHENOXYPHENYL) N PHENYLIMIDAZO[1,2 A]PYRIDIN 3 AMINE;
6 (6 FLUORO 1H BENZO[D]IMIDAZOL 2 YL) 2 (4 PHENOXYPHENYL) N PHENYLIMIDAZO[1,2 A]PYRIMIDIN 3 AMINE;
6 (6 FLUORO 1H BENZO[D]IMIDAZOL 2 YL) N PHENYL 2 (4 TOLYL)IMIDAZO[1,2 A]PYRIMIDIN 3 AMINE;
6 (6 PHENOXY 1H BENZO[D]IMIDAZOL 2 YL) N PHENYL 2 (4 TOLYL)IMIDAZO[1,2 A]PYRIDIN 3 AMINE;
6 [5 (4 BROMOPHENYL) 1H IMIDAZOL 2 YL] 2 (4 PHENOXYPHENYL) N PHENYLIMIDAZO[1,2 A]PYRIDIN 3 AMINE;
6 [5 (4 FLUOROPHENYL) 1,3,4 OXADIAZOL 2 YL] 2 (4 PHENOXYPHENYL) N PHENYLIMIDAZO[1,2 A]PYRIDIN 3 AMINE;
6 [5 (4 NITROPHENYL) 1,3,4 OXADIAZOL 2 YL] 2 (4 PHENOXYPHENYL) N PHENYLIMIDAZO[1,2 A]PYRIDIN 3 AMINE;
AMOXICILLIN;
ANTIINFECTIVE AGENT;
CEFEPIME;
IMIDAZO[1,2 A]PYRIDINE DERIVATIVE;
IMIDAZO[1,2 A]PYRIMIDINE DERIVATIVE;
UNCLASSIFIED DRUG;
UNINDEXED DRUG;
VANCOMYCIN;
ANTIBACTERIAL ACTIVITY;
ARTICLE;
BACTERIAL GROWTH;
CONTROLLED STUDY;
DRUG SYNTHESIS;
GRAM NEGATIVE BACTERIUM;
GRAM POSITIVE BACTERIUM;
MINIMUM INHIBITORY CONCENTRATION;
NONHUMAN;
STAPHYLOCOCCUS AUREUS;
STRUCTURE ACTIVITY RELATION;
ANTI-BACTERIAL AGENTS;
CELL PROLIFERATION;
GRAM-NEGATIVE BACTERIA;
GRAM-POSITIVE BACTERIA;
IMIDAZOLES;
MICROBIAL SENSITIVITY TESTS;
MOLECULAR STRUCTURE;
PYRIDINES;
PYRIMIDINES;
STEREOISOMERISM;
STRUCTURE-ACTIVITY RELATIONSHIP;
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EID: 78649319180
PISSN: 02235234
EISSN: 17683254
Source Type: Journal
DOI: 10.1016/j.ejmech.2010.09.049 Document Type: Article |
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Times cited : (93)
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References (33)
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