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dc.rights.licenseembargoen_US
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 3 LCPO : Polymer Self-Assembly & Life Sciences
dc.contributor.authorSALAS-AMBROSIO, Pedro
hal.structure.identifierLaboratoire de chimie de coordination [LCC]
hal.structure.identifierPathogénèse des Bactéries Anaérobies / Pathogenesis of Bacterial Anaerobes [PBA (U-Pasteur_6)]
dc.contributor.authorTRONNET, Antoine
hal.structure.identifierCentre d'Etudes et de Recherche sur le Médicament de Normandie [CERMN]
dc.contributor.authorSINCE, Marc
hal.structure.identifierPharmacochimie et Biologie pour le Développement [PHARMA-DEV]
dc.contributor.authorBOURGEADE-DELMAS, Sandra
hal.structure.identifierLaboratoire de chimie de coordination [LCC]
hal.structure.identifierUniversité Toulouse III - Paul Sabatier [UT3]
dc.contributor.authorSTIGLIANI, Jean-Luc
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 3 LCPO : Polymer Self-Assembly & Life Sciences
dc.contributor.authorVAX, Amelie
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 3 LCPO : Polymer Self-Assembly & Life Sciences
dc.contributor.authorLECOMMANDOUX, Sebastien
hal.structure.identifierInstitut Pasteur [Paris] [IP]
hal.structure.identifierPathogénèse des Bactéries Anaérobies / Pathogenesis of Bacterial Anaerobes [PBA (U-Pasteur_6)]
dc.contributor.authorDUPUY, Bruno
hal.structure.identifierLaboratoire de chimie de coordination [LCC]
hal.structure.identifierUniversité Toulouse III - Paul Sabatier [UT3]
dc.contributor.authorVERHAEGHE, Pierre
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 3 LCPO : Polymer Self-Assembly & Life Sciences
dc.contributor.authorBONDUELLE, Colin
IDREF: 134527046
dc.date.accessioned2021-03-18T14:33:02Z
dc.date.available2021-03-18T14:33:02Z
dc.date.issued2021-03-02
dc.identifier.issn0002-7863en_US
dc.identifier.urioai:crossref.org:10.1021/jacs.0c13231
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/26740
dc.description.abstractEnCyclic polymers display unique physicochemical and biological properties. However, their development is often limited by their challenging preparation. In this work, we present a simple route to cyclic poly(α-peptoids) from N-alkylated-N-carboxyanhydrides (NNCA) using LiHMDS promoted ring-expansion polymerization (REP) in DMF. This new method allows the unprecedented use of lysine-like monomers in REP to design bioactive macrocycles bearing pharmaceutical potential against Clostridioides difficile, a bacterium responsible for nosocomial infections.
dc.language.isoENen_US
dc.rightsAttribution-NonCommercial-ShareAlike 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/us/*
dc.sourcecrossref
dc.subjectRing expansion polymerization (REP)
dc.subject.enMacrocyclic polypeptoids
dc.subject.enClostridioides difficile
dc.title.enCyclic Poly(α-peptoid)s by Lithium bis(trimethylsilyl)amide (LiHMDS)-Mediated Ring-Expansion Polymerization: Simple Access to Bioactive Backbones
dc.typeArticle de revueen_US
dc.identifier.doi10.1021/jacs.0c13231en_US
dc.subject.halChimie/Polymèresen_US
dc.subject.halSciences du Vivant [q-bio]/Microbiologie et Parasitologie/Bactériologieen_US
dc.identifier.pubmed33651603en_US
bordeaux.journalJournal of the American Chemical Societyen_US
bordeaux.page3697-3702en_US
bordeaux.volume143en_US
bordeaux.issue10en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionBordeaux INPen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcedissemin
hal.identifierhal-03173586
hal.version1
hal.date.transferred2021-03-18T14:33:07Z
hal.exporttrue
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