Review of Synthetic Accessibility And Pharmacological Activity of 1,2,4-Triazole and 2-Methylbenzimidazole Derivatives

[1]  D. Astruc Introduction: Nanoparticles in Catalysis. , 2020, Chemical reviews.

[2]  Babak Mokhtari,et al.  Synthesis, in vitro antifungal evaluation and docking studies of novel derivatives of imidazoles and benzimidazoles , 2019, Medicinal Chemistry Research.

[3]  F. Gao,et al.  Antibacterial activity study of 1,2,4-triazole derivatives. , 2019, European journal of medicinal chemistry.

[4]  A. Abdelazeem,et al.  Design, Synthesis and Antiproliferative Evaluation of Novel 1,2,4-Triazole/Schiff Base Hybrids with EGFR and B-RAF Inhibitory Activities. , 2019, Anti-cancer agents in medicinal chemistry.

[5]  Shovan Mondal Recent advancement of Ullmann-type coupling reactions in the formation of C–C bond , 2016, ChemTexts.

[6]  Andreas Martin,et al.  Metal Nanoparticles as Emerging Green Catalysts , 2016 .

[7]  T. Lu,et al.  Discovery of potential anti-inflammatory drugs: diaryl-1,2,4-triazoles bearing N-hydroxyurea moiety as dual inhibitors of cyclooxygenase-2 and 5-lipoxygenase. , 2014, Organic & biomolecular chemistry.

[8]  S. R. Thakare,et al.  Room Temperature N-Arylation of 1,2,4-Triazoles under Ligand-Free Condition , 2012 .

[9]  Y. Bansal,et al.  The therapeutic journey of benzimidazoles: a review. , 2012, Bioorganic & medicinal chemistry.

[10]  Junhua Li,et al.  A highly efficient Cu-catalyst system for N-arylation of azoles in water , 2012 .

[11]  E. S. Coimbra,et al.  Thiopurine derivatives containing triazole and steroid: synthesis, antimalarial and antileishmanial activities. , 2011, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

[12]  M. Al-Dosari,et al.  Synthesis and in vitro anticancer evaluation of some novel hexahydroquinoline derivatives having a benzenesulfonamide moiety. , 2011, European journal of medicinal chemistry.

[13]  Vikas Sharma,et al.  Synthesis and pharmacological evaluation of novel 5-substituted-1-(phenylsulfonyl)-2-methylbenzimidazole derivatives as anti-inflammatory and analgesic agents. , 2010, European journal of medicinal chemistry.

[14]  N. Foroughifar,et al.  Synthesis of some novel Schiff bases containing 1,2,4-triazole ring , 2010 .

[15]  M. Taillefer,et al.  Catalytic C-C, C-N, and C-O Ullmann-type coupling reactions. , 2009, Angewandte Chemie.

[16]  G. Manolikakes Transition-Metal Catalyzed Cross-Coupling Reactions of Functionalized Organometallic Reagents, Nickel-Catalyzed Amination of Aryl Chlorides and Preparation and Reactions of Organozinc Reagents , 2009 .

[17]  V. Sorokin Copper (I) Catalyzed N-Arylation of Azoles, the Recent Developments , 2008 .

[18]  Chuanjie Cheng,et al.  Highly Practical “Ligand‐Free‐Like” Copper‐Catalyzed N‐Arylation of Azoles in Lower Nitrile Solvents , 2008 .

[19]  M. Taillefer,et al.  Catalytic C-C, C-N, and C-O Ullmann-type coupling reactions: copper makes a difference. , 2008, Angewandte Chemie.

[20]  C. Bolm,et al.  Ligand-Free Copper-Catalyzed N-Arylation of Nitrogen Nucleophiles , 2007 .

[21]  Gaocan Li,et al.  Simple copper salt-catalyzed N-arylation of nitrogen-containing heterocycles with aryl and heteroaryl halides. , 2007, The Journal of organic chemistry.

[22]  L. Rout,et al.  Efficient CuO-nanoparticle-catalyzed C-S cross-coupling of thiols with iodobenzene. , 2007, Angewandte Chemie.

[23]  S. Buchwald,et al.  Copper-catalyzed N-arylation of imidazoles and benzimidazoles. , 2007, The Journal of organic chemistry.

[24]  M. Taillefer,et al.  Highly efficient and mild copper-catalyzed N- and C-arylations with aryl bromides and iodides. , 2004, Chemistry.

[25]  K. Nagai,et al.  Synthesis and antibacterial activity of novel and potent DNA gyrase inhibitors with azole ring. , 2004, Bioorganic & medicinal chemistry.

[26]  S. Buchwald,et al.  Copper-diamine-catalyzed N-arylation of pyrroles, pyrazoles, indazoles, imidazoles, and triazoles. , 2004, The Journal of organic chemistry.

[27]  D. Denis,et al.  Benzimidazoles as new potent and selective DP antagonists for the treatment of allergic rhinitis. , 2004, Bioorganic & medicinal chemistry letters.

[28]  C. Avendaño,et al.  New synthetic applications of aryllead triacetates. N-arylation of azoles. , 1995 .

[29]  J. Major,et al.  New nonpeptide angiotensin II receptor antagonists. 1. Synthesis, biological properties, and structure-activity relationships of 2-alkyl benzimidazole derivatives. , 1992, Journal of medicinal chemistry.

[30]  Y. Ghasemi,et al.  Antibacterial Activity of Some New Azole Compounds , 2012 .