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dc.contributor.authorUeda, Yoshihiroen
dc.contributor.authorFuruta, Takumien
dc.contributor.authorKawabata, Takeoen
dc.contributor.alternative川端, 猛夫ja
dc.date.accessioned2015-12-16T02:35:12Z-
dc.date.available2015-12-16T02:35:12Z-
dc.date.issued2015-10-05-
dc.identifier.issn1433-7851-
dc.identifier.urihttp://hdl.handle.net/2433/202609-
dc.descriptionArticle first published online: 28 AUG 2015en
dc.description.abstractThe first total syntheses of multifidosides A-C have been achieved. The synthetic strategy is characterized by catalytic site-selective acylation of unprotected glycoside precursors in the final stage of the synthesis. High functional-group tolerance of the site-selective acylation, promoted by an organocatalyst, enabled the conventionally difficult molecular transformation in a predictable and reliable manner. An advantage of this strategy is to avoid the risks of undesired side reactions during the removal of the protecting groups at the final stage of the total synthesis.en
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherwileyen
dc.rightsThis is the peer reviewed version of the following article: Ueda, Y., Furuta, T. and Kawabata, T. (2015), Final-Stage Site-Selective Acylation for the Total Syntheses of Multifidosides A–C. Angew. Chem. Int. Ed., 54: 11966–11970, which has been published in final form at http://dx.doi.org/10.1002/anie.201504729. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving.en
dc.rightsThe full-text file will be made open to the public on 28 AUG 2016 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.subjectacylationen
dc.subjectglycosidesen
dc.subjectnatural productsen
dc.subjectorganocatalysisen
dc.subjectsynthetic methodsen
dc.titleFinal-Stage Site-Selective Acylation for the Total Syntheses of Multifidosides A-C.en
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.ncidAA0052535X-
dc.identifier.jtitleAngewandte Chemie: International Editionen
dc.identifier.volume54-
dc.identifier.issue41-
dc.identifier.spage11966-
dc.identifier.epage11970-
dc.relation.doi10.1002/anie.201504729-
dc.textversionauthor-
dc.startdate.bitstreamsavailable2016-08-28-
dc.identifier.pmid26384855-
dcterms.accessRightsopen access-
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