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dc.contributor.authorKobayashi, Yusukeen
dc.contributor.authorNakatsuji, Yuyaen
dc.contributor.authorLi, Shanjien
dc.contributor.authorTsuzuki, Seijien
dc.contributor.authorTakemoto, Yoshijien
dc.contributor.alternative小林, 祐輔ja
dc.contributor.alternative中辻, 雄哉ja
dc.contributor.alternative都築, 誠二ja
dc.contributor.alternative竹本, 佳司ja
dc.date.accessioned2019-07-18T06:08:10Z-
dc.date.available2019-07-18T06:08:10Z-
dc.date.issued2018-03-26-
dc.identifier.issn1433-7851-
dc.identifier.issn1521-3773-
dc.identifier.urihttp://hdl.handle.net/2433/243151-
dc.descriptionThis article also appears in: European Symposium on Organic Chemistry 2019en
dc.description.abstractUsing a halogen bond (XB) donor and Schreiner's thiourea as cooperative catalysts, various amides, including the asparagine residues of several peptides, were directly coupled with glycosyl trichloroacetimidates to give unique N‐acylorthoamides in good yields. Synthetic applications of N‐acylorthoamides, including rearrangement to the corresponding β‐N‐glycoside, were also demonstrated.en
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherWileyen
dc.rightsThis is the peer reviewed version of the following article: [Yusuke Kobayashi, Yuya Nakatsuji, Shanji Li, Seiji Tsuzuki, Yoshiji Takemoto. Direct N‐Glycofunctionalization of Amides with Glycosyl Trichloroacetimidate by Thiourea/Halogen Bond Donor Co‐Catalysis. Angewandte Chemie International Edition, 57(14), 3646-3650], which has been published in final form at https://doi.org/10.1002/anie.201712726. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.en
dc.rightsThe full-text file will be made open to the public on 25 March 2019 in accordance with publisher's 'Terms and Conditions for Self-Archiving'.en
dc.rightsThis is not the published version. Please cite only the published version.en
dc.rightsこの論文は出版社版でありません。引用の際には出版社版をご確認ご利用ください。ja
dc.subjectglycosylationen
dc.subjectorganocatalysten
dc.subjectXB donoren
dc.titleDirect N-Glycofunctionalization of Amides with Glycosyl Trichloroacetimidate by Thiourea/Halogen Bond Donor Co-Catalysisen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.ncidAA0052535X-
dc.identifier.jtitleAngewandte Chemieen
dc.identifier.volume57-
dc.identifier.issue14-
dc.identifier.spage3646-
dc.identifier.epage3650-
dc.relation.doi10.1002/anie.201712726-
dc.textversionauthor-
dc.addressGraduate School of Pharmaceutical Sciences, Kyoto Universityen
dc.addressGraduate School of Pharmaceutical Sciences, Kyoto Universityen
dc.addressGraduate School of Pharmaceutical Sciences, Kyoto Universityen
dc.addressResearch Initiative of Computational Sciences (RICS)・Nanosystem Research Institute (NRI), National Institute of Advanced Industrial Science and Technology (AIST)en
dc.addressGraduate School of Pharmaceutical Sciences, Kyoto Universityen
dc.identifier.pmid29412493-
dcterms.accessRightsopen access-
datacite.date.available2019-03-25-
datacite.awardNumber16H06384-
datacite.awardNumber17K15423-
dc.identifier.pissn1433-7851-
dc.identifier.eissn1521-3773-
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.funderName.alternativeJapan Society for the Promotion of Science (JSPS)en
jpcoar.funderName.alternativeJapan Society for the Promotion of Science (JSPS)en
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