Drupal-Biblio17<style face="normal" font="default" size="100%">Facile regioselective decomposition of tosylhydrazones: an application towards the synthesis of alpha-lipoic acid</style>Drupal-Biblio17<style face="normal" font="default" size="100%">First enantiospecific synthesis of (+)-beta-herbertenol</style>Drupal-Biblio17<style face="normal" font="default" size="100%">First enantiospecific synthesis of (-)-parvifoline and (-)-curcuquinone</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Facile total synthesis of (+/-)-alpha-cuparenone employing diallylation and RCM as key steps</style>Drupal-Biblio17<style face="normal" font="default" size="100%">First enantiospecific synthesis of (-)-heritol: absolute configuration determination</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Fluconazole analogues containing 2H-1,4-benzothiazin-3(4H)-one or 2H-1,4-benzoxazin-3(4H)-one moieties, a novel class of anti-Candida agents</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Formal synthesis of (+/-)-camptothecin via tricyclic lactone as key synthon</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Formal synthesis of (-)-stemoamide using a useful epimerization at C-8</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Facile and convenient synthesis of (+/-)-Biotin via MgCl2/Et3N-mediated C-C coupling and mitsunobu reaction</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Formal syntheses of (2R,3R)-3-hydroxy pipecolic acid and (2R,3S)-3-hydroxy pipecolic acid from L-ascorbic acid</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Formal synthesis of brivaracetam: a key to construct the pyrrolidone scaffold using Pd-catalyzed oxidative cyclization and ring-closing metathesis reaction</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Furan-derived chiral bicycloaziridino lactone synthon: collective syntheses of oseltamivir phosphate (Tamiflu), (S)-pipecolic acid and its 3-hydroxy derivatives</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Formal synthesis of (-)-quinagolide: diastereoselective ring expansion via a bicyclic aziridinium ion strategy to access the octahydrobenzo[g]quinoline architecture</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Formal Synthesis of Corynanthe Indole Alkaloid (±)-Mitralactonine: Construction of α-Hydroxy-Keto Functionalized Tetracyclic Skeleton</style>