Asutay, OktayHamarat, NiluferUludağ, NesimiCoşkun, Necdet2022-05-112022-05-1120150040-4039https://doi.org/10.1016/j.tetlet.2015.04.111https://hdl.handle.net/20.500.11776/5949Anhydrous Ce(SO4)(2) in chloroform selectively converts oximes into the parent carbonyl compounds in good yields. Hammett correlations helped to indicate a plausible mechanism for the above reaction. The formation of 1-(dinitromethyl)benzene was assumed to be a product of isonitroso hydrogen reaction with arylaldoximes. (C) 2015 Elsevier Ltd. All rights reserved.en10.1016/j.tetlet.2015.04.111info:eu-repo/semantics/closedAccessOxidationOximesReaction mechanismHammett correlationIsonitroso hydrogenParent Carbonyl-CompoundsOne-Pot SynthesisPreparative ConversionOximesEfficientRegenerationDerivativesNitrateSelective oxidative deoximation with anhydrous Ce(IV) sulfateArticle562539023904Q2WOS:0003565496000132-s2.0-84930181671Q3