Facile regioselective synthesis of novel bioactive thiazolyl-pyrazoline derivatives via a three-component reaction and their antimicrobial activity

Bioorganic and Medicinal Chemistry Letters

Volumn 23, Issue 2, 2013, Pages 548-551

  Sharifzadeh, Bahman ^a   Mahmoodi, Nosrat O ^a   Mamaghani, Manouchehr ^a   Tabatabaeian, Khalil ^a   Chirani, Alireza Salimi ^b   Nikokar, Iraj ^c  

^a UNIVERSITY OF GUILAN   (Iran)

^b SHAHID BEHESHTI UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^c GUILAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

Author keywords

Antibacterial activity; Chalcone; Thiazolyl pyrazoline; Thiosemicarbazide; Three component

Indexed keywords

2 (3,5 DIP TOLYL 4,5 DIHYDRO 1H PYRAZOL 1 YL) 4 PHENYLTHIAZOLE; 2 (3,5 DIPHENYL 4,5 DIHYDRO 1H PYRAZOL 1 YL) 4 PHENYLTHIAZOLE DERIVATIVE; 2 [3 (4 CHLOROPHENYL) 3,3A,4,5 TETRAHYDRO 2H BENZO[G]INDAZOL 2 YL] 4 PHENYLTHIAZOLE; 2 [3 (4 METHOXYPHENYL) 3,3A,4,5 TETRAHYDRO 2H BENZO[G]INDAZOL 2 YL] 4 PHENYLTHIAZOLE; 2 [3 (4 METHOXYPHENYL) 5 4 TOLYL 4,5 DIHYDRO 1H PYRAZOL 1 YL] 4 PHENYLTHIAZOLE; 2 [3,5 BIS(4 METHOXYPHENYL) 4,5 DIHYDRO 1H PYRAZOL 1 YL] 4 PHENYLTHIAZOLE; 2 [5 (4 METHOXYPHENYL) 3 4 TOLYL 4,5 DIHYDRO 1H PYRAZOL 1 YL] 4 PHENYLTHIAZOLE; 2 [5 (4 METHOXYPHENYL) 3 PHENYL 4,5 DIHYDRO 1H PYRAZOL 1 YL] 4 PHENYLTHIAZOLE; 4 PHENYL 2 [3 (THIOPHEN 2 YL) 3,3A,4,5 TETRAHYDRO 2H BENZO[G]INDAZOL 2 YL]THIAZOLE; 4 PHENYL 2 [3 PHENYL 5 (THIOPHEN 2 YL) 4,5 DIHYDRO 1H PYRAZOL 1 YL)THIAZOLE; BROMIDE; CHALCONE DERIVATIVE; GENTAMICIN; PHENACYL BROMIDE; PYRAZOLINE DERIVATIVE; THIAZOLE DERIVATIVE; THIOSEMICARBAZIDE; UNCLASSIFIED DRUG;

ANTIBACTERIAL ACTIVITY; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CATALYSIS; CONTROLLED STUDY; CRYSTAL STRUCTURE; CYCLOADDITION; DIASTEREOISOMER; DRUG STRUCTURE; DRUG SYNTHESIS; ESCHERICHIA COLI; INFRARED SPECTROSCOPY; NONHUMAN; ONE POT SYNTHESIS; PHARMACOPHORE; POLYMERIZATION; PROTON NUCLEAR MAGNETIC RESONANCE; PSEUDOMONAS AERUGINOSA; STAPHYLOCOCCUS AUREUS;

ANTI-INFECTIVE AGENTS; BACTERIA; CATALYSIS; MOLECULAR STRUCTURE; PYRAZOLES; STEREOISOMERISM; THIAZOLES;

EID: 84871719687     PISSN: 0960894X     EISSN: 14643405     Source Type: Journal    
DOI: 10.1016/j.bmcl.2012.11.024     Document Type: Article

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