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dc.rights.licenseopenen_US
dc.relation.isnodoublef68a456e-9b2e-4f65-a5ba-46d698f19805*
dc.relation.isnodouble911d4729-7a1e-4277-8aa3-99994a8d3caa*
dc.contributor.authorATCHER, Joan
dc.contributor.authorNAGAI, Aki
dc.contributor.authorMAURIZOT, Victor
dc.contributor.authorTANATANI, Aya
dc.contributor.authorHUC, Ivan
dc.date.accessioned2020-03-23T15:21:34Z
dc.date.available2020-03-23T15:21:34Z
dc.date.issued2019
dc.identifier.issn1359-7345en_US
dc.identifier.otherhttp://www.rsc.org/suppdata/c9/cc/c9cc04849a/c9cc04849a1.pdfen_US
dc.identifier.otherhttp://www.rsc.org/suppdata/c9/cc/c9cc04849a/c9cc04849a2.cifen_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/3932
dc.description.abstractEnThe preference of N,N-aryl, alkyl tertiary amides for cis conformations has been exploited through the use of tertiary squaramides as hairpin turn units that promote the folding of aromatic beta-sheets. Head-to-head aromatic arrangements were shown to prevail in sufficiently long bent aromatic sequences.
dc.language.isoENen_US
dc.titleAromatic beta-sheet foldamers based on tertiary squaramides
dc.typeArticle de revueen_US
dc.identifier.doi10.1039/c9cc04849a
dc.subject.halChimie/Matériauxen_US
bordeaux.journalChemical Communicationsen_US
bordeaux.page10392-10395en_US
bordeaux.volume55en_US
bordeaux.hal.laboratoriesInstitut de Chimie & de Biologie des Membranes & des Nano-objets (CBMN) - UMR 5248
bordeaux.issue70en_US
bordeaux.institutionBordeaux INPen_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.identifierhal-03184440
hal.version1
hal.date.transferred2021-03-29T12:41:44Z
hal.exporttrue
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