Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1762
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dc.contributor.authorTHADKE, SHIVAJI A.en_US
dc.contributor.authorKar, Mrityunjoyen_US
dc.contributor.authorSen Gupta, Sayamen_US
dc.contributor.authorHOTHA, SRINIVASen_US
dc.date.accessioned2019-02-14T05:49:14Z
dc.date.available2019-02-14T05:49:14Z
dc.date.issued2011-09en_US
dc.identifier.citationCarbohydrate Research, 346(12), 1511-1518en_US
dc.identifier.issn1873-426Xen_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1762-
dc.identifier.urihttps://doi.org/10.1016/j.carres.2011.04.018en_US
dc.description.abstractPropargyl glyco 1,2-orthoesters were exploited for the efficient synthesis of interesting glycomonomers such as glyco-acrylates and acrylamides using gold catalysts. It was observed that propargyl glyco 1,2-orthoesters with hydroxyethyl acrylates gives very good yield of the corresponding glyco-acrylates in a single step in the presence of catalytic amount of gold(III) catalyst; whereas, gold catalyzed glycosidation reaction on hydroxyethyl acrylamides was found to yield the corresponding acrylamidoyl 1,2-orthoester which was then converted to the corresponding glycol-acrylamide in the presence of catalytic amount of TMSOTf. Synthesized glyco-acrylate/acrylamide monomers are shown to undergo thiolate addition as well as free radical polymerization.en_US
dc.language.isoenen_US
dc.publisherElsevier B.V.en_US
dc.subjectGlycopolymersen_US
dc.subjectCarbohydratesen_US
dc.subjectGlycosylationen_US
dc.subjectGlycoacrylatesen_US
dc.subjectGlycoacrylamidesen_US
dc.subjectGolden_US
dc.subject2011en_US
dc.titleGold catalyzed glycosidations for the synthesis of sugar acrylate/acrylamide hybrids and their utilityen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleCarbohydrate Researchen_US
dc.publication.originofpublisherForeignen_US
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