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dc.contributor.authorVIDADALA, SRINIVASA RAOen_US
dc.contributor.authorGayatri, Gaddamannuguen_US
dc.contributor.authorSastry, G. Naraharien_US
dc.contributor.authorHOTHA, SRINIVASen_US
dc.date.accessioned2019-02-14T05:49:14Z
dc.date.available2019-02-14T05:49:14Z
dc.date.issued2011-08en_US
dc.identifier.citationChemical Communications, 47 (35), 9906-9908.en_US
dc.identifier.issn1359-7345en_US
dc.identifier.issn1364-548Xen_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1764-
dc.identifier.urihttps://doi.org/10.1039/C1CC13134Fen_US
dc.description.abstractTransfuranosylations are not well studied though many similar studies exist for transpyranosylation; herein, we report that propargyl/methyl D-ribf- and D-lyxf- give only 1,2-transglycosides whereas D-araf- and D-xylf- result in a mixture of 1,2-trans and 1,2-cisglycosides; observed facts are rationalised by computational studies.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectPropargyl/methyl furanosidesen_US
dc.subjectPotential glycosyl donorsen_US
dc.subjectTransfuranosylationsen_US
dc.subject1,2-cisglycosidesen_US
dc.subjectComputational studiesen_US
dc.subject2011en_US
dc.titlePropargyl/methyl furanosides as potential glycosyl donorsen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleChemical Communicationsen_US
dc.publication.originofpublisherForeignen_US
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