Drupal-Biblio17<style face="normal" font="default" size="100%">Copper-, ligand- and solvent-free synthesis of ynones by coupling acid chlorides with terminal alkynes</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Enantioselective synthesis of (+)-(S,S)-reboxetine</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Ionic liquid promoted facile one-pot synthesis of 1-pyridylimidazo[1,5-a]pyridines from dipyridylketone and aryl aldehydes</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Ligand-, copper-, and amine-free one-pot synthesis of 2-substituted indoles via Sonogashira coupling 5-endo-dig cyclization</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Efficient synthesis of 2,4-disubstituted thiazoles using ionic liquid under ambient conditions: a practical approach towards the synthesis of Fanetizole</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Enantioselective synthesis of (S)-dapoxetine</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Novel one-pot three-component synthesis of 2,4-disubstituted-3H-benzo[b][1,4]diazepines in water</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis and evaluation of antifungal properties of a series of the novel 2-amino-5-oxo-4-phenyl-5,6,7,8-tetrahydroquinoline-3-carbonitrile and its analogues</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of an indole containing KDR kinase inhibitor by tandem Sonogashira coupling-5-endo-dig-cyclization as a key step</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Catalyst-free efficient synthesis of 2-aminothiazoles in water at ambient temperature</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Efficient and eco-friendly synthesis of 2-amino-1,3-selenazoles in an ionic liquid/water system under ambient conditions</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Efficient synthesis of antifungal pyrimidines via palladium catalyzed Suzuki/Sonogashira cross-coupling reaction from Biginelli 3,4-dihydropyrimidin-2(1H)-ones</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Efficient synthesis of quinoxalines in the ionic liquid 1-n-butylimidazolium tetrafluoroborate ([Hbim]BF4) at ambient temperature</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Novel process for the synthesis of class I antiarrhythmic agent (+/-)-cibenzoline and its analogs</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Simple and efficient one-pot, three-component, solvent-free synthesis of beta-enaminones via sonogashira coupling-Michael addition sequences</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of tryptanthrin and deoxyvasicinone by a regioselective lithiation-intramolecular electrophilic reaction approach</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Ultrasound promoted copper-, ligand- and amine-free synthesis of benzo[b]furans/nitro benzo[b]furans via Sonogashira coupling-5-endo-dig-cyclization</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Proline-catalyzed simple and efficient synthesis of 1,8-dioxo-decahydroacridines in aqueous ethanol medium</style>