TY - JOUR
T1 - ZnO Nanocatalyst Mediated Convergent Synthesis of Highly Substituted Imidazole and Imidazole-derived Bi-heterocyclic Scaffolds as Potential Antibacterial Agents
AU - Jayashree, A.
AU - Narayana, B.
AU - Uppine, Gauthama B.
AU - Ghate, Vivek M.
AU - Lewis, Shaila A.
AU - Prakash, Bharathi
AU - Kunhanna, Sarojini B.
AU - Kumar, Madan S.
PY - 2019/9/1
Y1 - 2019/9/1
N2 - A new series of novel highly substituted imidazole and imidazole bi-heterocycles have been synthesized via atom economic, one-pot condensation reaction using benzil, substituted benzaldehydes, various amine scaffolds, and ammonium acetate using ZnO nanoparticles as effective catalyst. Simple operation, cheap catalyst, good to excellent yield, etc, are some of the advantages of this protocol. The characterization of the synthesized imidazole analogues was performed by Fourier transform infrared, nuclear magnetic resonance (1H and 13C), mass analysis, and elemental analysis. The structures were unequivocally confirmed by single-crystal X-ray diffraction analysis. Synthesized compounds were tested for antibacterial activities by resazurin reduction assay. All compounds tested showed significant activity against bacteria. Among the 24 compounds tested, compounds 1c, 1i, 2c, 2g, and 3a proved to be more active against the bacterial strain tested.
AB - A new series of novel highly substituted imidazole and imidazole bi-heterocycles have been synthesized via atom economic, one-pot condensation reaction using benzil, substituted benzaldehydes, various amine scaffolds, and ammonium acetate using ZnO nanoparticles as effective catalyst. Simple operation, cheap catalyst, good to excellent yield, etc, are some of the advantages of this protocol. The characterization of the synthesized imidazole analogues was performed by Fourier transform infrared, nuclear magnetic resonance (1H and 13C), mass analysis, and elemental analysis. The structures were unequivocally confirmed by single-crystal X-ray diffraction analysis. Synthesized compounds were tested for antibacterial activities by resazurin reduction assay. All compounds tested showed significant activity against bacteria. Among the 24 compounds tested, compounds 1c, 1i, 2c, 2g, and 3a proved to be more active against the bacterial strain tested.
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U2 - 10.1002/jhet.3627
DO - 10.1002/jhet.3627
M3 - Article
AN - SCOPUS:85070075010
SN - 0022-152X
VL - 56
SP - 2398
EP - 2410
JO - Journal of Heterocyclic Chemistry
JF - Journal of Heterocyclic Chemistry
IS - 9
ER -