dc.contributor.author |
Singh, Adesh Kumar |
|
dc.contributor.author |
Tiwari, Varsha |
|
dc.contributor.author |
Kunj Bihari, Mishra |
|
dc.contributor.author |
Gupta, Surabhi |
|
dc.contributor.author |
Kandasamy, Jeyakumar |
|
dc.date.accessioned |
2019-10-23T06:39:54Z |
|
dc.date.available |
2019-10-23T06:39:54Z |
|
dc.date.issued |
2017-05-23 |
|
dc.identifier.issn |
18605397 |
|
dc.identifier.uri |
http://localhost:8080/xmlui/handle/123456789/415 |
|
dc.description.abstract |
A 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.language.iso |
en |
en_US |
dc.publisher |
Beilstein-Institut Zur Forderung der Chemischen Wissenschaften |
en_US |
dc.subject |
monosaccharides; oxidation; sulfones; sulfoxides; thioglycosides; urea–hydrogen peroxide |
en_US |
dc.title |
Urea–hydrogen peroxide prompted the selective and controlled oxidation of thioglycosides into sulfoxides and sulfones |
en_US |
dc.type |
Article |
en_US |