Drupal-Biblio17<style face="normal" font="default" size="100%">Asymmetric total synthesis of eicosanoid</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Efficient and selective cleavage of the tert-butoxycarbonyl (Boc) group under basic condition</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Ring-closing metathesis mediated total synthesis of microcarpalide and herbarumin III</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Double intramolecular oxymercuration: stereoselective synthesis of highly substituted bis-tetrahydrofuran</style>Drupal-Biblio17<style face="normal" font="default" size="100%">General strategy for a short and efficient synthesis of 3-hydroxy-4-methylprolines (HMP)</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Stereoselective synthesis of the polyketide chain of nagahamide A</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of the spiro fused beta-lactone-gamma-lactam segment of oxazolomycin</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Protecting group directed ring-closing metathesis (RCM): the first total synthesis of an anti-malarial nonenolide</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Short and efficient synthetic strategy for the total syntheses of (S)-(+)- and (R)-(-)-Plakolide A</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Syntheis of unusual tricyclic ring systems of biological interest</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of the C19-C34 segment of amphidinolide C</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total syntheses of schulzeines B and C</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Towards the enantioselective synthesis of anti-HIV agents litseaverticillols C and K from D-glucose</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Carbohydrate templates for the synthesis of prototype renin inhibitors</style>Drupal-Biblio17<style face="normal" font="default" size="100%">First asymmetric total synthesis of penarolide sulfate A(1)</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Highly selective approach for the total synthesis of (+)-heliconol A</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Practical syntheses of 4-fluoroprolines</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Stereoselective synthesis of the C33-C44 fragment of palau'amide</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis of the C14-C29 segment of amphidinolide U utilizing a tandem dihydroxylation-S(N)2 cyclization protocol</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis of (S)-(-)-curvularin: a ring-closing-metathesis-based construction of the macrocyclic framework</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Click chemistry based rapid one-pot synthesis and evaluation for protease inhibition of new tetracyclic triazole fused benzodiazepine derivatives</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Highly stereoselective approach toward the synthesis of the macrolactone core of amphidinolide W</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Stereoselective synthesis of the densely functionalized C1-C9 fragment of amphidinolides C and F</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Syntheis of new chiral 5,6,7,8-tetrahydrotetrazolo[1,5-a]pyrazines from alpha-amino acid derivatives following ``click'' chemistry</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total syntheses and absolute stereochemistry of decarestrictines C-1 and C-2</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Stereoselective formal total synthesis of novel antibiotic (-)-centrolobine</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthetic studies of superstolide A: a carbohydrate based synthesis of the C21-C26 segment</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Carbohydrate-based synthesis of the C13-C22 fragment of amphidinolide X</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Practical syntheses of proposed and revised manzacidin B and their congeners</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis of isocladosporin and 3-epi-isocladosporin</style>