Drupal-Biblio17<style face="normal" font="default" size="100%">Convenient synthesis of the enantiomerically pure beta-blocker (S)-betaxolol using hydrolytic kinetic resolution</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Facile oxidation of flavanones to flavones using [hydroxy(tosyloxy)iodo]benzene in an ionic liquid</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Pictet-Spengler cyclization in room temperature ionic liquid: a convenient access to tetrahydro beta-carbolines</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Concise synthesis of beta-blockers (S)-metoprolol and (S)-betaxolol using hydrolytic kinetic resolution</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Thallium(III) p-tosylate mediated oxidative 2,3-aryl rearrangement: a new useful route to ipriflavone and its analogs</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Convenient synthesis of enantiomerically pure (R)-mexiletine using hydrolytic kinetic resolution method</style>Drupal-Biblio17<style face="normal" font="default" size="100%">First ionic liquid-promoted Kabbe condensation reaction for an expeditious synthesis of privileged bis-spirochromanone scaffolds</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Facile enantioselective synthesis of enantiomerically pure (R)-phenoxybenzamine hydrochloride using the hydrolytic kinetic resolution method</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%">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%">Chiral aziridine ring opening: facile synthesis of (R)-modletine and (R)-phenoxybenzamine hydrochloride</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Pharmacophore and docking based virtual screening of validated mycobacterium tuberculosis targets</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Alternate synthesis of appetite suppressant (R)-2-benzylmorpholine employing Sharpless asymmetric epoxidation strategy</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%">Thallium(III) p-tosylate-mediated oxidative [1,2] rearrangement of 2-naphthyl and 2-heteroarylchromanones</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>