dc.contributor.author |
KAYASTHA, ABHIJEET K. |
en_US |
dc.contributor.author |
HOTHA, SRINIVAS |
en_US |
dc.date.accessioned |
2019-07-23T11:08:16Z |
|
dc.date.available |
2019-07-23T11:08:16Z |
|
dc.date.issued |
2012-05 |
en_US |
dc.identifier.citation |
Chemical Communications, 48(57), 7161-7163. |
en_US |
dc.identifier.issn |
1359-7345 |
en_US |
dc.identifier.issn |
1364-548X |
en_US |
dc.identifier.uri |
http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3614 |
|
dc.identifier.uri |
https://doi.org/10.1039/C2CC32649C |
en_US |
dc.description.abstract |
Glycosidation with stable alkyl glycosyl donors using a catalytic amount of gold salts is promising. Herein, 1-ethynylcyclohexanyl glycosides are identified as novel donors at room temperature and mechanistic investigation showed that the leaving group simply extrudes out. |
en_US |
dc.language.iso |
en |
en_US |
dc.publisher |
Royal Society of Chemistry |
en_US |
dc.subject |
Chemistry |
en_US |
dc.subject |
2012 |
en_US |
dc.title |
Versatile gold catalyzed transglycosidation at ambient temperature |
en_US |
dc.type |
Article |
en_US |
dc.contributor.department |
Dept. of Chemistry |
en_US |
dc.identifier.sourcetitle |
Chemical Communications |
en_US |
dc.publication.originofpublisher |
Foreign |
en_US |