Synthesis and antimicrobial activity of pyrazolyl 1,3,4-oxadiazoles

Synthetic Communications

Volumn 40, Issue 4, 2010, Pages 482-493

  Padmavathi, Venkatapuram ^a   Reddy, Gali Sudhakar ^a   Reddy, Guda Dinneswara ^a   Payani, Thalari ^a  

^a SRI VENKATESWARA UNIVERSITY   (India)

Author keywords

1,3,4 oxadiazoles; 1,3 dipolar cycloaddition; Antimicrobial activity; Pyrazolines

Indexed keywords

5 (4 CHLOROBENZYLSULFONYLMETHYL) 2 (4',5' DIHYDRO 4' PHENYL 1'H PYRAZOL 3' YL) 1,3,4 OXADIAZOLE; 5 (4 CHLOROBENZYLSULFONYLMETHYL) 2 [4',5' DIHYDRO 4 (4 CHLOROPHENYL) 1'H PYRAZOL 3' YL] 1,3,4 OXADIAZOLE; 5 (4 CHLOROPHENYLSULFONYLMETHYL) 2 (4',5' DIHYDRO 4' PHENYL 1'H PYRAZOL 3' YL) 1,3,4 OXADIAZOLE; 5 (4 CHLOROPHENYLSULFONYLMETHYL) 2 [4',5' DIHYDRO 4' (4 CHLOROPHENYL) 1'H PYRAZOL 3' YL] 1,3,4 OXADIAZOLE; 5 (4 METHYLBENZYLSULFONYLMETHYL) 2 (4',5' DIHYDRO 4' PHENYL 1'H PYRAZOL 3' YL) 1,3,4 OXADIAZOLE; 5 (4 METHYLPHENYLSULFONYLMETHYL) 2 (4',5' DIHYDRO 4' PHENYL 1'H PYRAZOL 3' YL) 1,3,4 OXADIAZOLE; 5 (BENZYLSULFONYLMETHYL) 2 [4',5' DIHYDRO (4 CHLOROPHENYL) 1'H PYRAZOL 3' YL] 13,4, OXADIAZOLE; 5 (BENZYLSULFONYLMETHYL) 2 [4',5' DIHYDRO 4' PHENYL 1'H PYRAZOL 3' YL] 1,3,4 OXADIAZOLE; 5 (PHENYLSULFONYLMETHYL) 2 [4',5' DIHYDRO 4' (4 CHLOROPHENYL) 1'H PYRAZOL 3' YL] 1,3,4 OXADIAZOLE; 5 (PHENYLSULFONYLMETHYL) 2 [4',5' DIHYDRO 4' PHENYL 1'H PYRAZOL 3' YL] 1,3,4 OXADIAZOLE; ACETIC ACID; ANTIINFECTIVE AGENT; BENZYL DERIVATIVE; CHLORAMPHENICOL; ESTER; HETEROCYCLIC COMPOUND; KETOCONAZOLE; METHYL GROUP; OXADIAZOLE DERIVATIVE; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE; PYRAZOLE DERIVATIVE; UNCLASSIFIED DRUG;

AGAR DIFFUSION; ANTIBACTERIAL ACTIVITY; ANTIFUNGAL ACTIVITY; ARTICLE; ASPERGILLUS NIGER; BACILLUS SUBTILIS; CONTROLLED STUDY; CURVULARIA LUNATA; DRUG SCREENING; DRUG STRUCTURE; DRUG SYNTHESIS; FUSARIUM SOLANI; IN VITRO STUDY; KLEBSIELLA PNEUMONIAE; MINIMUM INHIBITORY CONCENTRATION; NONHUMAN; PROTEUS VULGARIS; STAPHYLOCOCCUS AUREUS; STEREOCHEMISTRY; SUBSTITUTION REACTION;

EID: 76149097529     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397910902985531     Document Type: Article

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