NaNO2-mediated transformation of aliphatic secondary nitroalkanes into ketones or oximes under neutral, aqueous conditions: How the nitro derivative catalyzes its …

…, C Matt, A Wagner, C Mioskowski

Index: Matt, Christophe; Wagner, Alain; Mioskowski, Charles Journal of Organic Chemistry, 1997 , vol. 62, # 2 p. 234 - 235

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Citation Number: 31

Abstract

The nitrosation of secondary nitro derivatives into ketones or oximes depending on the nitro substituents has been reinvestigated. The reaction efficiently takes place under neutral conditions, thus allowing acid-sensitive substrates to be converted in very good yields. The generation of nitrosating species under such mild conditions is unprecedented. Mechanistic investigations strongly suggest that they result from the nucleophilic attack of the nitrite ...