Drupal-Biblio17<style face="normal" font="default" size="100%">First total synthesis of hunanamycin A</style>Drupal-Biblio17<style face="normal" font="default" size="100%">General approach to N-heterocyclic carbenes with a fused tetracyclic core: ligands for suzuki-miyaura cross-coupling reaction</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Multi-gram scale synthesis of hunanamycin A, an antibiotic natural product from the marine source</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Repurposing of a drug scaffold: identification of novel sila analogues of rimonabant as potent antitubercular agents</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Route to benzimidazol-2-ones via decarbonylative ring contraction of quinoxalinediones: application to the synthesis of flibanserin, A drug for treating hypoactive sexual desire disorder in women and marine natural product hunanamycin analogue</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis of an anticancer natural product (+/-)-peharmaline A and its analogues</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Antibiotic natural product hunanamycin A: Lead identification towards anti-Salmonella agents</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Identification of new modulator of DNA repairing pathways based on natural product (±)-peharmaline A</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Synthesis, biological evaluation and docking studies of silicon incorporated diarylpyrroles as MmpL3 inhibitors: an effective strategy towards development of potent anti-tubercular agents</style>