Publication : Preparation of N-substituted N-arylsulfonylglycines and their use in peptoid synthesis
bul.rights.dateAccepPubl | 2015-11-09 | fr_CA |
bul.rights.periodeEmbargo | P1Y | fr_CA |
bul.rights.typeDate | datePublication | fr_CA |
dc.audience | Professeurs (Enseignement supérieur) | fr_CA |
dc.audience | Étudiants | fr_CA |
dc.audience | Doctorants | fr_CA |
dc.audience | Biochimistes | fr_CA |
dc.contributor.author | Biron, Éric | |
dc.contributor.author | Jobin, Steve | |
dc.contributor.author | Herby, Claire | |
dc.contributor.author | Vézina-Dawod, Simon | |
dc.contributor.author | Derson, Antoine | |
dc.date.accessioned | 2016-04-27T17:41:15Z | |
dc.date.available | 2016-11-09T05:00:00Z | |
dc.date.issued | 2015-11-09 | |
dc.description.abstract | To 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.doi | 10.1021/acs.orglett.5b02862 | fr_CA |
dc.identifier.issn | 1523-7060 | fr_CA |
dc.identifier.pubmed | 26550851 | fr_CA |
dc.identifier.uri | http://hdl.handle.net/20.500.11794/879 | |
dc.language | eng | fr_CA |
dc.publisher | American Chemical Society | fr_CA |
dc.rights | http://purl.org/coar/access_right/c_abf2 | |
dc.subject.rvm | Peptides | fr_CA |
dc.subject.rvm | Monomères | fr_CA |
dc.subject.rvm | Composés organiques -- Synthèse | fr_CA |
dc.subject.rvm | Peptoïdes | fr_CA |
dc.title | Preparation of N-substituted N-arylsulfonylglycines and their use in peptoid synthesis | fr_CA |
dc.type | article de recherche | |
dc.type.legacy | COAR1_1::Texte::Périodique::Revue::Contribution à un journal::Article::Article de recherche | |
dcterms.bibliographicCitation | Organic letters, Vol. 17 (22), 5626-5629 (2015) | fr_CA |
dspace.accessstatus.time | 2024-03-25 18:06:57 | |
dspace.entity.type | Publication | |
relation.isAuthorOfPublication | 18b333cd-28ac-4a91-b46a-01e33876ce31 | |
relation.isAuthorOfPublication | 1d079ab5-bce4-4050-bb17-4f1ae0f9890f | |
relation.isAuthorOfPublication | 768a911d-63d3-4aee-85c4-c8c17c42b59a | |
relation.isAuthorOfPublication.latestForDiscovery | 18b333cd-28ac-4a91-b46a-01e33876ce31 | |
relation.isResourceTypeOfPublication | 4c433ef5-3937-4530-8252-cca17d715747 | |
relation.isResourceTypeOfPublication.latestForDiscovery | 4c433ef5-3937-4530-8252-cca17d715747 | |
rioxxterms.project | 371503-2010 | fr_CA |
rioxxterms.project.funder-name | Natural Sciences and Engineering Research Council of Canada | fr_CA |
rioxxterms.version | Accepted Manuscript (AM) | fr_CA |
rioxxterms.version-of-record | https://doi.org/10.1021/acs.orglett.5b02862 | fr_CA |
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