Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/62787
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dc.contributor.authorWanniang, Kmendashisha-
dc.contributor.authorLipon, Tyrchain Mitre-
dc.contributor.authorMarpna, Ibakyntiew D-
dc.contributor.authorShangpliang, Shangpliang-
dc.contributor.authorMyrboh, Bekington-
dc.contributor.authorNongkhlaw, R L-
dc.date.accessioned2023-10-19T05:00:28Z-
dc.date.available2023-10-19T05:00:28Z-
dc.date.issued2023-10-
dc.identifier.issn2583-1321 (Online); 0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/62787-
dc.description1103-1107en_US
dc.description.abstractA new method portraying the utility of lead tetraacetate as an oxidizing agent in the synthesis of α-sulfonyloxyketones from aryl ketones and sulfonic acids has been described. This methodology offers a new alternative for the synthesis of a series of α-sulfonyloxyketones with broad substrate scope, easy availability of reactants as well as the use of simple oxidant.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR, Indiaen_US
dc.sourceIJC Vol.62(10) [October 2023]en_US
dc.subjectOxidationen_US
dc.subjectα-Sulfonyloxyketonesen_US
dc.subjectAryl ketonesen_US
dc.subjectSulfonic acidsen_US
dc.subjectLead tetraacetateen_US
dc.titleOxidative α-sulfonyloxylation of aryl ketones with sulfonic acids by lead tetraacetateen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.56042/ijc.v62i10.6190en_US
Appears in Collections:IJC Vol.62(10) [October 2023]

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