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%">Overcoming the lack of oral availability of cyclic hexapeptides: design of a selective and orally available ligand for the integrin alpha v beta 3</style>Drupal-Biblio17<style face="normal" font="default" size="100%">From a helix to a small cycle: metadynamics-inspired alpha v beta 6 integrin selective ligands</style>Drupal-Biblio17<style face="normal" font="default" size="100%">N-Heterocyclic carbene-catalyzed michael-michael-lactonization cascade for the enantioselective synthesis of tricyclic delta-lactones</style>Drupal-Biblio17<style face="normal" font="default" size="100%">N-Methylation of isoDGR peptides: discovery of a selective alpha 5 beta 1-integrin ligand as a potent tumor imaging agent</style>Drupal-Biblio17<style face="normal" font="default" size="100%"> Systematic synthesis of a 6-component organic-salt alloy of naftopidil, and pentanary, quaternary and ternary multicomponent crystals</style>Drupal-Biblio17<style face="normal" font="default" size="100%">N-Heterocyclic carbene-catalyzed umpolung of imines for the enantioselective synthesis of dihydroquinoxalines</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Selective targeting of integrin alpha v beta 8 by a highly active cyclic peptide</style>Drupal-Biblio17<style face="normal" font="default" size="100%">EGCG impedes human Tau aggregation and interacts with Tau</style>Drupal-Biblio17<style face="normal" font="default" size="100%">HDAC6 ZnF UBP as the modifier of tau structure and function</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Melatonin interacts with repeat domain of Tau to mediate disaggregation of paired helical filaments</style>Drupal-Biblio17<style face="normal" font="default" size="100%">N-heterocyclic carbene catalysis exploiting oxidative imine umpolung for the generation of imidoyl azoliums</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Novel cilengitide-based cyclic RGD peptides as alpha nu beta(3) integrin inhibitors</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Residue-based propensity of aggregation in the Tau amyloidogenic hexapeptides AcPHF6*and AcPHF6</style>Drupal-Biblio17<style face="normal" font="default" size="100%">[1,3]-Claisen rearrangement via removable functional group mediated radical stabilization</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Possible fine-tuning of methane activation toward C2 oxygenates by 3d-transition metal-ions doped nano-ceria-zirconia</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Total synthesis, structure elucidation and expanded bioactivity of icosalide A: effect of lipophilicity and ester to amide substitution on its bioactivity</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Integrating 3,4-Dihydro-2H-1,4-oxazine into peptides as a modification: silver triflate-catalyzed cyclization of N-Propargyl N-Sulfonyl amino alcohols for SPPS applications </style>Drupal-Biblio17<style face="normal" font="default" size="100%">Macrocyclic peptides derived from AcPHF6*and AcPHF6 to selectively modulate the Tau aggregation</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Metal-free one-pot domino synthesis of oxazolidinethione derivatives of quaternary amino acids from α-amino esters and aldehydes using CS2</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Graphene oxide-cyclopentylamine (GO-d-CP) liquid crystals as a novel alignment medium for anisotropic nmr with analyte recovery</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Ketenimine multicomponent strategy for multifaceted amidine functionalization of peptides on the solid phase</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Peptide functionalization with dithioate and trithioate groups: A CS2-mediated solid-phase approach</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Peptide-triazolobenzodiazepine hybrids: a catalyst-free on-resin strategy to build complex therapeutic motifs into peptides</style>