Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2505
Full metadata record
DC FieldValueLanguage
dc.contributor.authorTHADKE, SHIVAJI A.en_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.issued2016-07en_US
dc.identifier.citationCarbohydrate Research, 430, 16-23.en_US
dc.identifier.issn0008-6215en_US
dc.identifier.issn1873-426Xen_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2505-
dc.identifier.urihttps://doi.org/10.1016/j.carres.2016.04.022en_US
dc.description.abstractThe O-glycosidation of hydroxysuccinimides and hydroxyphthalimides with a variety of aldose derived propargyl 1,2-orthoesters under the gold(III)-catalyzed glycosidation conditions is reported. A wide range of hydroxysuccinimidyl and hydroxyphthalimidyl glycosides were synthesized from corresponding glycosyl orthoesters including glucosyl, mannosyl, galactosyl, ribofuranosyl, arabinofuranosyl, lyxofuranosyl and xylofuranosyl using gold catalysis repertoire. The protocol is identified to be compatible for the synthesis of aminooxy glycosides of higher oligosaccharides as well.en_US
dc.language.isoenen_US
dc.publisherElsevier B.V.en_US
dc.subjectGold catalysisen_US
dc.subjectGlycosidesen_US
dc.subjectOligosaccharidesen_US
dc.subjectChemical synthesisen_US
dc.subjectHigher oligosaccharidesen_US
dc.subject2016en_US
dc.titleFacile synthesis of aminooxy glycosides by gold(III)-catalyzed glycosidationen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleCarbohydrate Researchen_US
dc.publication.originofpublisherForeignen_US
Appears in Collections:JOURNAL ARTICLES

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.