Drupal-Biblio17<style face="normal" font="default" size="100%">Green synthetic route to antimalarial and antibacterial agent CJ-15,801 and its isomer cis-CJ-15,801</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Studies toward the synthesis of potent anti-inflammatory peptides solomonamides A and B: synthesis of a macrocyclic skeleton and key fragment 4-amino-6-(2 `-amino-4 `-hydroxyphenyl)-3-hydroxy-2-methyl-6-oxohexanoic acid (AHMOA)</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis of an anticancer norsesquiterpene alkaloid isolated from the fungus flammulina velutipes</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis of deoxy-solomonamide B by mimicking biogenesis</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Breaking and making of olefins simultaneously using ozonolysis: application to the synthesis of useful building blocks and macrocyclic core of solomonamides</style>Drupal-Biblio17<style face="normal" font="default" size="100%">One-pot quadruple/triple reaction sequence: a useful tool for the synthesis of natural products</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Enantiospecific formal synthesis of inthomycin C</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Molecules with O-acetyl group protect protein glycation by acetylating lysine residues</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis of the marine natural product solomonamide B necessitates stereochemical revision</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Access to a stereoisomer library of solomonamide macrocycles</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Comprehensive study on solomonamides: total synthesis, stereochemical revision, and SAR studies toward identification of simplified lead</style>