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- W2186121753 abstract "An elegant synthesis of newer desired aminobenzylated triphenyl imidazole hybrids is described. Cyclization of benzil with appropriate aromatic aldehydes in the presence of ammonium acetate yielded 2‐substit uted ‐ 4, 5‐diphenyl imidazole entities, which further undergoes mannich condensation reaction with benzaldehyde and various aromatic secondary amines afforded the title compounds. The constituents of the newly synthesised compounds have been established on the basis of their physical and spectral data. All the newly synthesised heterocycles have been screened for invitro antimicrobial and anti‐inflammatory activities. Among all the synthesized compounds, the compound TPI‐IV exhibited good anti‐inflammatory activity and better anti‐microbial activity against bacterial strains Staphylococcus aureus, Pseudomonas aeruginosa and fungal strain Candida albicans." @default.
- W2186121753 created "2016-06-24" @default.
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- W2186121753 date "2011-01-01" @default.
- W2186121753 modified "2023-09-27" @default.
- W2186121753 title "EXPLORING THE EFFECTS OF NEWER THREE COMPONENT AMINOBENZYLATED REACTIONS OF TRIPHENYL IMIDAZOLE MOTIF AS POTENT ANTIMICROBIAL AND ANTIINFLAMMATORY AGENTS" @default.
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