Synthesis of quinoline coupled [1,2,3]-triazoles as a promising class of anti-tuberculosis agents

Carbohydrate Research

Volumn 346, Issue 14, 2011, Pages 2084-2090

  Karthik Kumar, K ^a   Prabu Seenivasan, S ^b   Kumar, Vanaja ^b   Mohan Das, T ^a  

^a UNIVERSITY OF MADRAS   (India)

^b NATIONAL INSTITUTE FOR RESEARCH IN TUBERCULOSIS   (India)

Author keywords

Anti tubercular activity; Click chemistry; Cu(I) catalysed; Mycobacterium tuberculosis H37Rv; Quinoline derivatives; Saccharide triazole derivatives

Indexed keywords

ANTI-TUBERCULAR ACTIVITY; CLICK CHEMISTRY; MYCOBACTERIUM TUBERCULOSIS H37RV; QUINOLINE DERIVATIVE; TRIAZOLE DERIVATIVES;

ACETYLENE; CATALYSIS; NITROGEN COMPOUNDS; SUGARS; SYNTHESIS (CHEMICAL);

IODINE;

2 [(4 PHENYL 1H 1,2,3 TRIAZOL 1 YL)METHYL]QUINOLINE; 2 [[4 [(2,3 DI O ACETYL 4,6 O BUTYLIDENE BETA DEXTRO GLUCOPYRANOSYLOXY)METHYL] 1H 1,2,3 TRIAZOL 1 YL]METHYL]QUINOLINE; 2 [[4 [(2,3 DI O ACETYL 4,6 O ETHYLIDENE BETA DEXTRO GLUCOPYRANOSYLOXY)METHYL] 1H 1,2,3 TRIAZOL 1 YL]METHYL]QUINOLINE; 2 [[4 [(2,3,4 TRI O ACETYL BETA DEXTRO RIBOPYRANOSYLOXY)METHYL] 1H1,2,3 TRIAZOL 1 YL]METHYL]QUINOLINE; 2 [[4 [(2,3,4,6 TETRA O ACETYL ALPHA DEXTRO MANNOPYRANOSYLXY)METHYL] 1H 1,2,3 TRIAZOL 1 YL]METHYL]QUINOLINE; 2 [[4 [(2,3,4,6 TETRA O ACETYL BETA DEXTRO GALACTOPYRANOSYLOXY)METHYL] 1H 1,2,3 TRIAZOL 1 YL]METHYL]QUINOLINE; 2 [[4 [(2,3,4,6 TETRA O ACETYL BETA DEXTRO GLUCOPYRANOSYLOXY)METHYL] 1H 1,2,3 TRIAZOL 1 YL]METHYL]QUINOLINE; ALKYNE DERIVATIVE; CUPROUS ION; LUCIFERASE; QUINOLINE DERIVED ANTIINFECTIVE AGENT; RIFAMPICIN; TRIAZOLE DERIVATIVE; TUBERCULOSTATIC AGENT; UNCLASSIFIED DRUG;

ANTIBACTERIAL ACTIVITY; ARTICLE; CATALYSIS; CONTROLLED STUDY; DRUG POTENCY; DRUG SCREENING; DRUG SYNTHESIS; MINIMUM INHIBITORY CONCENTRATION; MYCOBACTERIUM TUBERCULOSIS; NONHUMAN; PRIORITY JOURNAL; STRUCTURE ACTIVITY RELATION;

ANTITUBERCULAR AGENTS; MYCOBACTERIUM TUBERCULOSIS; QUINOLINES; TRIAZOLES;

MYCOBACTERIUM TUBERCULOSIS;

EID: 80052756054     PISSN: 00086215     EISSN: 1873426X     Source Type: Journal    
DOI: 10.1016/j.carres.2011.06.028     Document Type: Article

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