Drupal-Biblio17<style face="normal" font="default" size="100%">Expedient synthesis of 1,2,3-triazole-fused tetracyclic compounds by intramolecular Huisgen ('click') reactions on carbohydrate-derived azido-alkynes</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of bile acid dimers linked with 1,2,3-triazole ring at C-3, C-11, and C-24 positions</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Design and synthesis of fluconazole/bile acid conjugate using click reaction</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Syntheis of unusual tricyclic ring systems of biological interest</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Functionalization of single-walled carbon nanotubes with azides derived from amino acids using click chemistry</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Assembly of gold nanoparticles on single-walled carbon nanotubes by using click chemistry</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Syntheis of new chiral 5,6,7,8-tetrahydrotetrazolo[1,5-a]pyrazines from alpha-amino acid derivatives following ``click'' chemistry</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis and biological evaluation of new 2-chloro-3-((4-phenyl-1H-1,2,3-triazol-1-yl)methyl)quinoline derivatives via click chemistry approach</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis and characterization of polyurethane-grafted single-walled carbon nanotubes via click chemistry</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Click chemistry: 1,2,3-triazoles as pharmacophores</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Syntheses and biological evaluation of new triazole-spirochromone conjugates as inhibitors of mycobacterium tuberculosis</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Topochemical click reaction: spontaneous self-stitching of a monosaccharide to linear oligomers through lattice-controlled azide-alkyne cycloaddition</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Facile strategy for synthesis of ,-heterobifunctionalized poly (epsilon-caprolactones) and poly (methyl methacrylate)s containing ``clickable'' aldehyde and allyloxy functional groups using initiator approach</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis, biological evaluation and molecular docking of novel coumarin incorporated triazoles as antitubercular, antioxidant and antimicrobial agents</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Clickable polyurethanes based on s- triazine ring containing aromatic diisocyanate bearing pendent alkyne group: synthesis and postmodification</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Aromatic polyesters containing pendant azido groups: synthesis, characterization, chemical modification and thermal cross-linking</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Click chemistry based multicomponent approach in the synthesis of spirochromenocarbazole tethered 1,2,3-triazoles as potential anticancer agents</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Thermally crosslinkable and chemically modifiable aromatic polyesters possessing pendant propargyloxy groups</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Enolate-mediated regioselective synthesis of 1,2,3-triazoles via azide-aldehydes or ketones [3+2]-cycloaddition reactions in aqueous phase</style>