dc.contributor.author |
THADKE, SHIVAJI A. |
en_US |
dc.contributor.author |
Kar, Mrityunjoy |
en_US |
dc.contributor.author |
Sen Gupta, Sayam |
en_US |
dc.contributor.author |
HOTHA, SRINIVAS |
en_US |
dc.date.accessioned |
2019-02-14T05:49:14Z |
|
dc.date.available |
2019-02-14T05:49:14Z |
|
dc.date.issued |
2011-09 |
en_US |
dc.identifier.citation |
Carbohydrate Research, 346(12), 1511-1518 |
en_US |
dc.identifier.issn |
1873-426X |
en_US |
dc.identifier.uri |
http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1762 |
|
dc.identifier.uri |
https://doi.org/10.1016/j.carres.2011.04.018 |
en_US |
dc.description.abstract |
Propargyl glyco 1,2-orthoesters were exploited for the efficient synthesis of interesting glycomonomers such as glyco-acrylates and acrylamides using gold catalysts. It was observed that propargyl glyco 1,2-orthoesters with hydroxyethyl acrylates gives very good yield of the corresponding glyco-acrylates in a single step in the presence of catalytic amount of gold(III) catalyst; whereas, gold catalyzed glycosidation reaction on hydroxyethyl acrylamides was found to yield the corresponding acrylamidoyl 1,2-orthoester which was then converted to the corresponding glycol-acrylamide in the presence of catalytic amount of TMSOTf. Synthesized glyco-acrylate/acrylamide monomers are shown to undergo thiolate addition as well as free radical polymerization. |
en_US |
dc.language.iso |
en |
en_US |
dc.publisher |
Elsevier B.V. |
en_US |
dc.subject |
Glycopolymers |
en_US |
dc.subject |
Carbohydrates |
en_US |
dc.subject |
Glycosylation |
en_US |
dc.subject |
Glycoacrylates |
en_US |
dc.subject |
Glycoacrylamides |
en_US |
dc.subject |
Gold |
en_US |
dc.subject |
2011 |
en_US |
dc.title |
Gold catalyzed glycosidations for the synthesis of sugar acrylate/acrylamide hybrids and their utility |
en_US |
dc.type |
Article |
en_US |
dc.contributor.department |
Dept. of Chemistry |
en_US |
dc.identifier.sourcetitle |
Carbohydrate Research |
en_US |
dc.publication.originofpublisher |
Foreign |
en_US |