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dc.contributor.authorANTUNES, Stephanie
dc.contributor.authorDOUAT, Celine
dc.contributor.authorGUICHARD, Gilles
IDREF: 084339268
dc.date.accessioned2020-09-03T07:56:05Z
dc.date.available2020-09-03T07:56:05Z
dc.date.issued2016
dc.identifier.issn1434-193X
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/10817
dc.description.abstractEnThe introduction of a thiourea unit at a selected position in the backbone of aliphatic N,N-linked urea foldamers can be used to locally modulate the secondary structure and physicochemical properties. To facilitate scanning the effect of thiourea introduction into biologically active oligourea helices, we have investigated the solid-phase synthesis of oligoureas containing a single oxo-to-thioxo replacement in their sequence. Several suitably protected activated monomers were considered, and conditions for their coupling and deprotection were evaluated and compared. The synthesis of oligo(thio)ureas on TFA-labile resins (i.e., Rink amide resin; TFA = trifluoroacetic acid) required careful optimization, and the choice of N-Fmoc-aminoalkyl isothiocyanates (Fmoc = fluorenylmethoxycarbonyl) as monomers for thiourea-bond formation was found to be critical.
dc.language.isoen
dc.title.enSolid-Phase Synthesis of Hybrid Urea Oligomers Containing Conservative Thiourea Mutations
dc.typeArticle de revue
dc.identifier.doi10.1002/ejoc.201600177
dc.subject.halChimie/Matériaux
bordeaux.journalEUROPEAN JOURNAL OF ORGANIC CHEMISTRY
bordeaux.page2131-2138
bordeaux.hal.laboratoriesInstitut de Chimie & de Biologie des Membranes & des Nano-objets (CBMN) - UMR 5248*
bordeaux.hal.laboratoriesInstitut de Chimie & de Biologie des Membranes & des Nano-objets (CBMN, UMR 5248)
bordeaux.issue12
bordeaux.institutionUniversité de Bordeaux
bordeaux.institutionBordeaux INP
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