Drupal-Biblio17<style face="normal" font="default" size="100%">Efficient method for the synthesis of acylals from aldehydes under solvent-free conditions catalyzed by antimony trichloride</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis and in vitro study of 14-aryl-14H-dibenzo[a.j]xanthenes as cytotoxic agents</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Simple and efficient synthesis of 2-Aryl-2,3-dihydroquinolin-4(1H)-ones using silica chloride as a new catalyst under solvent-free conditions</style>Drupal-Biblio17<style face="normal" font="default" size="100%">First asymmetric synthesis of the antiepileptic drug lacosamide (Vimpat (R)) based on a hydrolytic kinetic resolution strategy</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%">Alternate synthesis of enantiomerically pure levetiracetam (Keppra (R))</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Efficient bakers' yeast-catalyzed multicomponent synthesis of -aminophosphonates in one pot</style>Drupal-Biblio17<style face="normal" font="default" size="100%">New enantioselective synthesis of the anticonvulsant drug pregabalin (lyrica) based on a hydrolytic kinetic resolution method</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis and antitubercular activity of amino alcohol fused spirochromone conjugates</style>Drupal-Biblio17<style face="normal" font="default" size="100%">New enantioselective synthesis of (S)-2-ethoxy-3-(4-hydroxyphenyl)Propanoic acid esters (EEHP and IEHP), useful pharmaceutical intermediates of PPAR agonists</style>Drupal-Biblio17<style face="normal" font="default" size="100%">New enantioselective synthesis of the anti-parkinson agent safinamide</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Spirochromone-chalcone conjugates as antitubercular agents: synthesis, bio evaluation and molecular modeling studies</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Efficient synthesis of the opioid analgesic (R)-phenampromide via an aziridinium ion</style>Drupal-Biblio17<style face="normal" font="default" size="100%">New and efficient enantioselective synthesis of both enantiomers of the calcium channel blocker bepridil</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Efficient synthesis of optically active herbicide (S)-metolachlor via reductive ring opening of 2-methoxymethylaziridine</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Cu-catalyzed multicomponent reaction of arylhydrazines with β-ketoesters and TBN: one-pot access to N 2-aryl 1,2,3-triazole-1-oxides</style>