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Article: Synthesis of cyclogentiotriose by macrocyclization via a ring-closing glycosylation.

TitleSynthesis of cyclogentiotriose by macrocyclization via a ring-closing glycosylation.
Authors
Issue Date2014
PublisherElsevier. The Journal's web site is located at http://www.elsevier.com/locate/tetlet
Citation
Tetrahedron Letters, 2014, v. 55 n. 40, p. 5525-5528 How to Cite?
AbstractThe synthesis of a benzylated cyclogentiotriose was achieved through the ring-closing glycosylation, which was developed by us recently. Moderate b-selectivity (3.3:1) was obtained in the 1,6 glycosidic linkage formation step. The a-acetoxy ether precursor was generated through the Rychnovsky reductive acetylation of a linear trisaccharide derived macrolactone.
Persistent Identifierhttp://hdl.handle.net/10722/210690

 

DC FieldValueLanguage
dc.contributor.authorLiu, H-
dc.contributor.authorLi, XC-
dc.date.accessioned2015-06-23T05:47:15Z-
dc.date.available2015-06-23T05:47:15Z-
dc.date.issued2014-
dc.identifier.citationTetrahedron Letters, 2014, v. 55 n. 40, p. 5525-5528-
dc.identifier.urihttp://hdl.handle.net/10722/210690-
dc.description.abstractThe synthesis of a benzylated cyclogentiotriose was achieved through the ring-closing glycosylation, which was developed by us recently. Moderate b-selectivity (3.3:1) was obtained in the 1,6 glycosidic linkage formation step. The a-acetoxy ether precursor was generated through the Rychnovsky reductive acetylation of a linear trisaccharide derived macrolactone.-
dc.languageeng-
dc.publisherElsevier. The Journal's web site is located at http://www.elsevier.com/locate/tetlet-
dc.relation.ispartofTetrahedron Letters-
dc.rightsNOTICE: this is the author’s version of a work that was accepted for publication in [Journal title]. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in PUBLICATION, [VOL#, ISSUE#, (DATE)] DOI#-
dc.titleSynthesis of cyclogentiotriose by macrocyclization via a ring-closing glycosylation.-
dc.typeArticle-
dc.identifier.emailLi, XC: xuechenl@hku.hk-
dc.identifier.emailLiu, H: liuhan@hku.hk-
dc.identifier.authorityLi, XC=rp00742-
dc.identifier.doi10.1016/j.tetlet.2014.08.063-
dc.identifier.hkuros243696-
dc.identifier.volume55-
dc.identifier.issue40-
dc.identifier.spage5525-
dc.identifier.epage5525-

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