Synthesis of quinoline coupled [1,2,3]-triazoles as a promising class of anti-tuberculosis agents
2011/06/30 by K. Karthik Kumar, S. Prabu Seenivasan, Vanaja Kumar +2 · 10 citations
Chemistry · Medicine · #Click Chemistry and Applications #HIV/AIDS drug development and treatment #Synthesis and Biological Evaluation
paper · doi:10.1016/j.carres.2011.06.028
Cited by
- Cu(I)-Catalyzed Click Chemistry in Glycoscience and Their Diverse Applications
- Electrolytic copper as cheap and effective catalyst for one-pot triazole synthesis. [europepmc]
- CuBr-ZnI 2 Combo-Catalysis for Mild Cu I -Cu III Switching and sp 2 C-H Activated Rapid Cyclization to Quinolines and Their Sugar-Based Chiral Analogues: A UV-Vis and XPS Study. [europepmc]
- Azidophosphonium salt-directed chemoselective synthesis of ( E )/( Z )-cinnamyl-1 H -triazoles and regiospecific access to bromomethylcoumarins from Morita-Baylis-Hillman adducts. [europepmc]
- Ciprofloxacin-Tethered 1,2,3-Triazole Conjugates: New Quinolone Family Compounds to Upgrade Our Antiquated Approach against Bacterial Infections. [europepmc]
- Gas-phase UV absorption spectra and OH-oxidation kinetics of 1 H -1,2,3-triazole and pyrazole. [europepmc]
- Quinolone: a versatile therapeutic compound class. [europepmc]
- Pd-, Cu-, and Ni-Catalyzed Reactions: A Comprehensive Review of the Efficient Approaches towards the Synthesis of Antibacterial Molecules. [europepmc]
- Synthesis of 1,2,3-Triazole and Tetrazole Appended Glycoconjugates Based on 3,6-Anhydroglucofuranose via Click Reaction. [europepmc]
- Structural Bias Effect On Azidation at C‑1 and C‑2 of Alkyl-3,6-anhydro‑d‑hexofuranosides: Synthetic Approach to Natural Products and Derivatives. [europepmc]