*Corresponding author:
S Muralikrishna, Biological E.Ltd company, shameerpet, Hyderabad, IndiaReceived: April 28, 2018; Published: May 08,2018
DOI: 10.26717/BJSTR.2018.04.001047
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SYNTHESIS AND BIOLOGICAL EVALUATION OF 1-(5-((9H-carbazol-9-yl)methyl)-2-methyl-1,3,4-oxadiazol-3(2H)-yl)ethanonering were synthesized by the condensation of 2-(9H-carbazol-9-yl)acetohydrazide with 2-(9H-carbazol-9-yl)-N’-ethylideneacetohydrazide and acetic anhydride. To this reaction was subjected. It forms 2-(1-((4-acetyl-5-methyl-5-(trifluoromthyl)-4,5-dihyro-1,3,4-oxadiazol-2-yl)methyl)-1Hindol -3yl)-3-(p-tolyl)thiazolidin-4-one.The structure of these newly synthesized compounds were characterised by 1H NMR,13CNMR ,Mass ,IR, and elemental analysis.
Keywords: 1, 3, 4oxadiazole; Acetic anhydride; Carboxazole
Abstract| Introduction| Synthesis of 2-(9H-Carbazol-9-yl)-N’-Ethylideneacetohydrazide( 3)| Anti-Bacterial Activity| Antifungal activity| References|