Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/694
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dc.contributor.authorSingh, Krishna Nand-
dc.contributor.authorKumar, Rajesh-
dc.contributor.authorShukla, Ajay Kumar-
dc.date.accessioned2008-04-03T09:49:42Z-
dc.date.available2008-04-03T09:49:42Z-
dc.date.issued2007-08-
dc.identifier.issn0376-4699-
dc.identifier.urihttp://hdl.handle.net/123456789/694-
dc.description1347-1351en_US
dc.description.abstractTetraethylammonium superoxide, generated in situ by the phase-transfer reaction of potassium superoxide and tetraethyl-ammonium bromide in DMF, brings about an easy cleavage of vicinal diols and related dihydroxy arenes under mild reaction conditions, at room temperature.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.sourceIJCB Vol.46B(8) [August 2007]en_US
dc.subjectTetraethylammonium superoxideen_US
dc.subject1,2-diolsen_US
dc.subjectDihydroxy arenesen_US
dc.subjectPhase-transfer catalysten_US
dc.subjectCleavage reactionen_US
dc.titleAn efficient C-C bond cleavage of 1,2-diols using tetraethylammonium superoxideen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.46B(08) [August 2007]

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