a b s t r a c tThe new analogs of benzimidazole fused heterocyclic compounds such as triazinane and oxadiazinanes were synthesised by classical amino methylation with different aryl-N,N 0 unsymmetrical thioureas. The antibacterial activity of triazinane and oxadiazinane compounds have been assessed with zone of inhibition by well diffusion method using a panel of selected gram positive and gram negative bacterial strains and which have showed good activity. The synthesised molecules were subjected to molecular docking studies with two proteins, namely topoisomerase II (PDB ID: 1JIJ) and DNA gyrase subunit b (PDB ID : 1KZN). The molecular docking studies are supporting the antibacterial activity exhibiting high inhibition constant and binding energy. Ó 2017 Mansoura University. Production and hosting by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
A new and efficient methodology to synthesize N-substituted pyrrole derivatives by Clauson Kaas reaction employing Oxone as catalyst was developed. The transformation was performed in acetonitrile under microwave irradiation. This procedure has several advantages such as high yield, clean product formation, and short reaction time.
Synthesis of 6,7-Dihydroxy-3-aryl-5-undecyl-4,1,2-benzoxadiazines. -Title compounds (VI) are obtained in a three-step procedure starting from embelin (I). The base used for deacetylation in the last step is not specified. The biological testing for antifungal and antibacterial activity is briefly described. Aryl-substituted benzoxadiazines show activity against Bacillus subtilis, E. coli and Proteus vulgaris. -(BRAHMESHWARI, G.; Indian J.
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