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A highly efficient TEMPO mediated oxidation of sugar primary alcohols into uronic acids using 1-chloro-1,2-benziodoxol-3(1H)-one at room temperature
| dc.contributor.author | Tiwari V.; Badavath V.N.; Singh A.K.; Kandasamy J. | |
| dc.date.accessioned | 2025-05-24T09:31:58Z | |
| dc.description.abstract | Oxidation of various sugar primary alcohols into corresponding uronic acids was demonstrated using 1-chloro-1,2-benziodoxol-3(1H)-one and TEMPO. The reaction proceeds at room temperature in good to excellent yields. Primary alcohols get oxidized selectively over the secondary alcohols under mild reaction conditions. © 2018 Elsevier Ltd | |
| dc.identifier.doi | https://doi.org/10.1016/j.tetlet.2018.05.021 | |
| dc.identifier.uri | http://172.23.0.11:4000/handle/123456789/17586 | |
| dc.relation.ispartofseries | Tetrahedron Letters | |
| dc.title | A highly efficient TEMPO mediated oxidation of sugar primary alcohols into uronic acids using 1-chloro-1,2-benziodoxol-3(1H)-one at room temperature |