Click chemistry inspired synthesis of piperazine-triazole derivatives and evaluation of their antimicrobial activities

[1]  O. Santos-Filho,et al.  Design, synthesis, and antiviral activity of new 1H-1,2,3-triazole nucleoside ribavirin analogs , 2014, Medicinal Chemistry Research.

[2]  Anil Kumar,et al.  Click Chemistry Inspired Structural Modification of Azole Antifungal Agents to Synthesize Novel “Drug Like” Molecules. , 2013 .

[3]  Anil Kumar,et al.  Click chemistry inspired structural modification of azole antifungal agents to synthesize novel ‘drug like’ molecules , 2012 .

[4]  V. Lima,et al.  Synthesis and Anti-Inflammatory Activity of New Alkyl-Substituted Phthalimide 1H-1,2,3-Triazole Derivatives , 2012, TheScientificWorldJournal.

[5]  Kan Wang,et al.  Chemistry and Biology of Multicomponent Reactions , 2012 .

[6]  Wei Wang,et al.  Chemistry and biology of multicomponent reactions. , 2012, Chemical reviews.

[7]  Jingli Hou,et al.  The impact of click chemistry in medicinal chemistry , 2012, Expert opinion on drug discovery.

[8]  V. Pore,et al.  Synthesis and antifungal activity of 1,5-disubstituted-1,2,3-triazole containing fluconazole analogues , 2012 .

[9]  V. Pore,et al.  Click Chemistry: 1,2,3‐Triazoles as Pharmacophores , 2012 .

[10]  Yan Zou,et al.  Synthesis, in vitro evaluation and molecular docking studies of new triazole derivatives as antifungal agents. , 2011, Bioorganic & medicinal chemistry letters.

[11]  Shabana I. Khan,et al.  Synthesis of 4‐aminoquinoline‐1,2,3‐triazole and 4‐aminoquinoline‐1,2,3‐triazole‐1,3,5‐triazine Hybrids as Potential Antimalarial Agents , 2011, Chemical biology & drug design.

[12]  Suman Gupta,et al.  Synthesis and evaluation of new furanyl and thiophenyl azoles as antileishmanial agents. , 2011, European journal of medicinal chemistry.

[13]  Yulan Chen,et al.  An Efficient One-Pot Synthesis of Heterocycle-Fused 1,2,3-Triazole Derivatives as Anticancer Agents. , 2011 .

[14]  Cheng-He Zhou,et al.  Synthesis of novel sulfanilamide-derived 1,2,3-triazoles and their evaluation for antibacterial and antifungal activities. , 2010, European journal of medicinal chemistry.

[15]  Yulan Chen,et al.  An efficient one-pot synthesis of heterocycle-fused 1,2,3-triazole derivatives as anti-cancer agents. , 2010, Bioorganic & medicinal chemistry letters.

[16]  C. Locht,et al.  Exploring drug target flexibility using in situ click chemistry: application to a mycobacterial transcriptional regulator. , 2010, ACS chemical biology.

[17]  K. Kirshenbaum,et al.  Tricks with Clicks: Modification of Peptidomimetic Oligomers via Copper-Catalyzed Azide—Alkyne [3 + 2] Cycloadition , 2010 .

[18]  K. Kirshenbaum,et al.  Tricks with clicks: modification of peptidomimetic oligomers via copper-catalyzed azide-alkyne [3 + 2] cycloaddition. , 2010, Chemical Society reviews.

[19]  Ahmed Kamal,et al.  Synthesis of 1,2,3-triazole-linked pyrrolobenzodiazepine conjugates employing 'click' chemistry: DNA-binding affinity and anticancer activity. , 2008, Bioorganic & medicinal chemistry letters.

[20]  S. Yıldız,et al.  Synthesis and antimicrobial activity of some novel phenyl and benzimidazole substituted benzyl ethers. , 2007, Bioorganic & medicinal chemistry letters.

[21]  Min Zhang,et al.  Structure-based optimization of azole antifungal agents by CoMFA, CoMSIA, and molecular docking. , 2006, Journal of medicinal chemistry.

[22]  H. Kolb,et al.  The growing impact of click chemistry on drug discovery. , 2003, Drug discovery today.

[23]  M. G. Finn,et al.  Click Chemistry: Diverse Chemical Function from a Few Good Reactions. , 2001, Angewandte Chemie.

[24]  M. Genin.  Substituent Effects on the Antibacterial Activity of Nitrogen—Carbon‐Linked (Azolylphenyl)oxazolidinones with Expanded Activity Against the Fastidious Gram‐Negative Organisms Haemophilus influenzae and Moraxella catarrhalis. , 2000 .

[25]  G A Petsko,et al.  Chemistry and biology. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[26]  D. Sheehan,et al.  Current and Emerging Azole Antifungal Agents , 1999, Clinical Microbiology Reviews.

[27]  E. Anaissie,et al.  The new antifungal azoles: fluconazole and itraconazole , 1994 .

[28]  E. De Clercq,et al.  1,2,3-Triazole-[2',5'-bis-O-(tert-butyldimethylsilyl)-beta-D- ribofuranosyl]-3'-spiro-5"-(4"-amino-1",2"-oxathiole 2",2"-dioxide) (TSAO) analogues: synthesis and anti-HIV-1 activity. , 1994, Journal of medicinal chemistry.

[29]  P. Chattaraj,et al.  Substituent effects. , 2005, The journal of physical chemistry. A.

[30]  M Reza Ghadiri,et al.  Heterocyclic peptide backbone modifications in an alpha-helical coiled coil. , 2004, Journal of the American Chemical Society.

[31]  J. Séguéla,et al.  Aromatic ethers of 1-aryl 2-(1H-azolyl)ethanol: study of antifungal activity , 1995 .