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dc.contributor.authorMishra, Bijoyanandaen_US
dc.contributor.authorNeralkar, Maheshen_US
dc.contributor.authorHOTHA, SRINIVASen_US
dc.date.accessioned2019-04-26T09:12:31Z
dc.date.available2019-04-26T09:12:31Z
dc.date.issued2016-06en_US
dc.identifier.citationAngewandte Chemie International Edition, 128(27), 7917-7922.en_US
dc.identifier.issn1433-7851en_US
dc.identifier.issn1521-3773en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2504-
dc.identifier.urihttps://doi.org/10.1002/ange.201511695en_US
dc.description.abstractGebefreudige Donoren: Stabile Alkinylcarbonatglykoside wurden als exzellente Glykosyldonoren identifiziert, die mit einem Au‐Ag‐Katalysator zur schnellen Synthese von Glykosiden, Nukleosiden und Oligosacchariden aktiviert werden können. Wiederholte Glykosidierungen mit Carbonat‐Glykosyldonoren ermöglichten die konvergente Synthese eines Tridecasaccharids.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectStable Alkynylen_US
dc.subjectGlycosyl Carbonatesen_US
dc.subjectCatalytic Anomericen_US
dc.subjectTridecasaccharide Reminiscenten_US
dc.subjectMycobacterium tuberculosisen_US
dc.subjectCell Wall Lipoarabinomannanen_US
dc.subject2016en_US
dc.titleStable Alkynyl Glycosyl Carbonates: Catalytic Anomeric Activation and Synthesis of a Tridecasaccharide Reminiscent of Mycobacterium tuberculosis Cell Wall Lipoarabinomannanen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleAngewandte Chemie International Editionen_US
dc.publication.originofpublisherForeignen_US
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