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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | SURESHKUMAR, GOPALSAMY | 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 | 2012-06 | en_US |
| dc.identifier.citation | Glycoconjugate Journal, 29(4), 221-230. | en_US |
| dc.identifier.issn | 0282-0080 | en_US |
| dc.identifier.issn | 1573-4986 | en_US |
| dc.identifier.uri | http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3613 | - |
| dc.identifier.uri | https://doi.org/10.1007/s10719-012-9400-7 | en_US |
| dc.description.abstract | Tetrasaccharide cap present in lipophosphoglycan of the Leishmania donovani responsible for visceral Leishmaniaisis is synthesized as a fully protected propargyl glycoside. AuBr3 mediated selective glycosylation of propargyl 1,2-orthoester in the presence of propargyl glycoside is employed as a key step to obtain propargyl containing oligomers. Further, propargyl tetrasaccharide is connected with a long chain hydrocarbon containing azidothiol functionality situated at two terminal ends via ‘click’ reaction. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Springer Nature | en_US |
| dc.subject | Glycosidation | en_US |
| dc.subject | Leishmania | en_US |
| dc.subject | Gold catalysis | en_US |
| dc.subject | Orthoester | en_US |
| dc.subject | Lipophosphoglycan | en_US |
| dc.subject | Tetrasaccharide | en_US |
| dc.subject | 2012 | en_US |
| dc.title | AuBr3 mediated glycosidations: synthesis of tetrasaccharide motif of the Leishmania donovani lipophosphoglycan | en_US |
| dc.type | Article | en_US |
| dc.contributor.department | Dept. of Chemistry | en_US |
| dc.identifier.sourcetitle | Glycoconjugate Journal | en_US |
| dc.publication.originofpublisher | Foreign | en_US |
| Appears in Collections: | JOURNAL ARTICLES | |
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