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Publication :
Preparation of N-substituted N-arylsulfonylglycines and their use in peptoid synthesis

bul.rights.dateAccepPubl2015-11-09fr_CA
bul.rights.periodeEmbargoP1Yfr_CA
bul.rights.typeDatedatePublicationfr_CA
dc.audienceProfesseurs (Enseignement supérieur)fr_CA
dc.audienceÉtudiantsfr_CA
dc.audienceDoctorantsfr_CA
dc.audienceBiochimistesfr_CA
dc.contributor.authorBiron, Éric
dc.contributor.authorJobin, Steve
dc.contributor.authorHerby, Claire
dc.contributor.authorVézina-Dawod, Simon
dc.contributor.authorDerson, Antoine
dc.date.accessioned2016-04-27T17:41:15Z
dc.date.available2016-11-09T05:00:00Z
dc.date.issued2015-11-09
dc.description.abstractTo increase the chemical diversity accessible with peptoids and peptide–peptoid hybrids, N-alkylated arylsulfonamides were used to prepare side chain protected N-substituted glycines compatible with solid-phase synthesis. The described procedures give access to peptoid monomers bearing a wide variety of functional groups from commercially available amines in four straightforward steps. The prepared N-substituted N-arylsulfonylglycines were used as monomers in solid-phase synthesis to introduce relevant functionalized side chains into peptoid oligomers and peptide–peptoid hybrids.fr_CA
dc.identifier.doi10.1021/acs.orglett.5b02862fr_CA
dc.identifier.issn1523-7060fr_CA
dc.identifier.pubmed26550851fr_CA
dc.identifier.urihttp://hdl.handle.net/20.500.11794/879
dc.languageengfr_CA
dc.publisherAmerican Chemical Societyfr_CA
dc.rightshttp://purl.org/coar/access_right/c_abf2
dc.subject.rvmPeptidesfr_CA
dc.subject.rvmMonomèresfr_CA
dc.subject.rvmComposés organiques -- Synthèsefr_CA
dc.subject.rvmPeptoïdesfr_CA
dc.titlePreparation of N-substituted N-arylsulfonylglycines and their use in peptoid synthesisfr_CA
dc.typearticle de recherche
dc.type.legacyCOAR1_1::Texte::Périodique::Revue::Contribution à un journal::Article::Article de recherche
dcterms.bibliographicCitationOrganic letters, Vol. 17 (22), 5626-5629 (2015)fr_CA
dspace.accessstatus.time2024-03-25 18:06:57
dspace.entity.typePublication
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relation.isAuthorOfPublication1d079ab5-bce4-4050-bb17-4f1ae0f9890f
relation.isAuthorOfPublication768a911d-63d3-4aee-85c4-c8c17c42b59a
relation.isAuthorOfPublication.latestForDiscovery18b333cd-28ac-4a91-b46a-01e33876ce31
relation.isResourceTypeOfPublication4c433ef5-3937-4530-8252-cca17d715747
relation.isResourceTypeOfPublication.latestForDiscovery4c433ef5-3937-4530-8252-cca17d715747
rioxxterms.project371503-2010fr_CA
rioxxterms.project.funder-nameNatural Sciences and Engineering Research Council of Canadafr_CA
rioxxterms.versionAccepted Manuscript (AM)fr_CA
rioxxterms.version-of-recordhttps://doi.org/10.1021/acs.orglett.5b02862fr_CA

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