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Urea–hydrogen peroxide prompted the selective and controlled oxidation of thioglycosides into sulfoxides and sulfones

dc.contributor.authorSingh, Adesh Kumar
dc.contributor.authorTiwari, Varsha
dc.contributor.authorKunj Bihari, Mishra
dc.contributor.authorGupta, Surabhi
dc.contributor.authorKandasamy, Jeyakumar
dc.date.accessioned2019-10-23T06:39:54Z
dc.date.available2019-10-23T06:39:54Z
dc.date.issued2017-05-23
dc.description.abstractA practical method for the selective and controlled oxidation of thioglycosides to corresponding glycosyl sulfoxides and sulfones is reported using urea–hydrogen peroxide (UHP). A wide range of glycosyl sulfoxides are selectively achieved using 1.5 equiv of UHP at 60 °C while corresponding sulfones are achieved using 2.5 equiv of UHP at 80 °C in acetic acid. Remarkably, oxidation susceptible olefin functional groups were found to be stable during the oxidation of sulfide.en_US
dc.identifier.issn18605397
dc.identifier.urihttps://idr-sdlib.iitbhu.ac.in/handle/123456789/415
dc.language.isoenen_US
dc.publisherBeilstein-Institut Zur Forderung der Chemischen Wissenschaftenen_US
dc.subjectmonosaccharides; oxidation; sulfones; sulfoxides; thioglycosides; urea–hydrogen peroxideen_US
dc.titleUrea–hydrogen peroxide prompted the selective and controlled oxidation of thioglycosides into sulfoxides and sulfonesen_US
dc.typeArticleen_US

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