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dc.contributor.authorLi, Shanjien
dc.contributor.authorKobayashi, Yusukeen
dc.contributor.authorTakemoto, Yoshijien
dc.contributor.alternative小林, 祐輔ja
dc.contributor.alternative竹本, 佳司ja
dc.date.accessioned2018-12-28T05:53:02Z-
dc.date.available2018-12-28T05:53:02Z-
dc.date.issued2018-06-01-
dc.identifier.issn0009-2363-
dc.identifier.urihttp://hdl.handle.net/2433/235932-
dc.description.abstractThrough the synergistic catalytic effect of the halogen bond (XB) donor and thiourea catalyst, a direct α-selective N-glycosylation of the amide residue of asparagine derivative was achieved using readily accessible glycosyl trichloroacetimidate. n-Butyl methyl ether was found to be the most suitable solvent for the α-selectivity.en
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherPharmaceutical Society of Japanen
dc.rights© 2018 The Pharmaceutical Society of Japan.en
dc.subjectglycosylationen
dc.subjectorganocatalysten
dc.subjecthalogen bonden
dc.subjecthydrogen bonden
dc.subjectgreen chemistryen
dc.titleOrganocatalytic direct α-selective N-glycosylation of amide with glycosyl trichloroacetimidateen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.ncidAA00602100-
dc.identifier.jtitleChemical and Pharmaceutical Bulletin-
dc.identifier.volume66-
dc.identifier.issue7-
dc.identifier.spage768-
dc.identifier.epage770-
dc.relation.doi10.1248/cpb.c18-00255-
dc.textversionpublisher-
dc.addressGraduate School of Advanced Integrated Studies in Human Survivability, Kyoto Universityen
dc.addressGraduate School of Pharmaceutical Sciences, Kyoto Universityen
dc.addressGraduate School of Advanced Integrated Studies in Human Survivability, Kyoto University・Graduate School of Pharmaceutical Sciences, Kyoto Universityen
dc.identifier.pmid29962459-
dcterms.accessRightsopen access-
datacite.awardNumber16H06384-
jpcoar.funderName日本学術振興会ja
jpcoar.funderName.alternativeJapan Society for the Promotion of Science (JSPS)en
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