Drupal-Biblio17<style face="normal" font="default" size="100%">Stereospecific route to 5,11-methanomorphanthridine alkaloids via intramolecular 1,3-dipolar cycloaddition of nonstabilized azomethine ylide: Formal total synthesis of (+/-)-pancracine</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Beta-lactam-azasugar hybrid as a competitive potent galactosidase inhibitor</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Construction of enantiopure pyrrolidine ring system via asymmetric [3+2]-cycloaddition of azomethine ylides</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Convergent approach toward the synthesis of the stereoisomers of C-6 homologues of 1-deoxynojirimycin and their analogues: evaluation as specific glycosidase inhibitors</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis and evaluation of 1-deoxy-8-epi-castanospermine, 1-deoxy-8-hydroxymethyl castanospermine, and (6S,7S,8R,8aR)-8-amino-octahydroindolizine-6,7-diol</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Suzuki cross-coupling and intramolecular aza-michael addition reaction sequence towards the synthesis of 1,10b-epi-7-deoxypancratistatins and their cytotoxicity studies</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Suzuki cross-coupling/reductive debenzyloxycarbonylation sequence for the syntheses of [c]annulated isoquinolines: application for the syntheses of pancratistatin-like isoquinolines</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of polyhydroxy piperidines and their analogues: a novel approach towards selective inhibitors of alpha-glucosidase</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Use of enantiomerically pure 7-azabicyclo[2.2.1]heptan-2-ol as a chiral template for the synthesis of aminocyclitols</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Enantioselective total synthesis of (2S,3R,4R)-D-xylo-phytosphingosine from substituted azetidin-2-one</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Stereoselective one-step construction of vicinal quaternary and tertiary stereocenters of the 5,10b-ethanophenanthridine skeleton: total synthesis of (+/-)-maritidine</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of polyfunctional quinolizidine alkaloids: development towards selective glycosidase inhibitors</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of optically pure 2,3,4-trisubstituted tetrahydrofurans via a two-step sequential Michael-Evans aldol cyclization strategy: total synthesis of (+)-magnolone</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Construction of the 5,10b-phenanthridine skeleton using [3+2]-cycloaddition of a non-stabilized azomethine ylide: total synthesis of (+/-)-maritidine and (+/-)-crinine alkaloids</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Enantioselective total syntheses of (-)-isonitramine, (-)-sibirine, and (+)-nitramine by ring-closing metathesis</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Iminium ion cascade reaction in the total synthesis of (+)-vincadifformine</style>Drupal-Biblio17<style face="normal" font="default" size="100%">One-step stereospecific strategy for the construction of the core structure of the 5,11-methanomorphanthridine alkaloids in racemic as well as in optically pure form: synthesis of (+/-)-pancracine and (+/-)-brunsvigine</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Temperature-guided diastereoselectivity switch during the desymmetrization of meso-7-azabicyclo[2.2.1]heptadiene: new strategy towards the synthesis of aminocyclitols</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Dimethyl [(2R,3R,5S)-5-phenylmorpholine-2,3-diyl]diacetate as a designer substrate in the syntheses of important heterocyclic scaffolds</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Organocatalytic dynamic kinetic resolution via conjugate addition: synthesis of chiral trans-2,5-dialkylcyclohexanones</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Stereoselective construction of 5,11-methanomorphanthridine and 5,10b-phenanthridine structural frameworks: total syntheses of (+/-)-pancracine, (+/-)-brunsvigine, (+/-)-maritidine, and (+/-)-crinine</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Visible light photoredox catalysis: generation and addition of N-aryltetrahydroisoquinoline-derived alpha-amino radicals to michael acceptors</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Alpha-trimethylsilylmethylamine radical cation in the synthesis of cyclic amines and beyond</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Efficient access to enantiopure 1,3-disubstituted isoindolines from selective catalytic fragmentation of an original desymmetrized rigid overbred template</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Efficient strategy for the construction of both enantiomers of the octahydropyrroloquinolinone ring system: total synthesis of (+)-aspidospermidine</style>Drupal-Biblio17<style face="normal" font="default" size="100%"> p-Selective (sp(2))-C-H functionalization for an acylation/alkylation reaction using organic photoredox catalysis</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis of (+)-trans- dihydronarciclasine from (+)-7-azabicyclo[2.2.1]heptanone</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of 2-azabicyclo[m.n.0]-alkanes and their application towards the synthesis of strychnos and stemona classes of alkaloids</style>