An efficient C-C bond cleavage of 1,2-diols using tetraethylammonium superoxide

dc.contributor.author	Singh K.N.; Kumar R.; Shukla A.K.
dc.date.accessioned	2025-05-24T09:58:20Z
dc.description.abstract	Tetraethylammonium superoxide, generated in situ by the phase-transfer reaction of potassium superoxide and tetraethylammonium bromide in DMF, brings about an easy cleavage of vicinal diols and related dihydroxy arenes under mild reaction conditions, at room temperature.
dc.identifier.doi	DOI not available
dc.identifier.uri	http://172.23.0.11:4000/handle/123456789/23190
dc.relation.ispartofseries	Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry
dc.title	An efficient C-C bond cleavage of 1,2-diols using tetraethylammonium superoxide

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