Highly Efficient Cu(I)-Catalyzed Oxidation of Alcohols to Ketones and Aldehydes with Diaziridinone
Organic Letters2013Vol. 15(5), pp. 992–995
Citations Over TimeTop 10% of 2013 papers
Abstract
A novel and efficient Cu(I)-catalyzed oxidation of alcohols has been achieved with di-tert-butyldiaziridinone as the oxidant under mild conditions. A wide variety of primary and secondary alcohols with various functional groups can be oxidized to aldehydes and ketones in high yields. The reaction proceeds under neutral conditions making it compatible with acid- or base-sensitive substrates, and it is amenable to gram scale.
Related Papers
- → Parallel recognition by virtue of differentiation between ketone and aldehyde(1998)13 cited
- Progress in synthesis and modification of ketone-aldehyde resin(2006)
- Discussion on oxidation of aldehyde and ketone(2001)
- The Synthesis of 2-Furyltriisopropoxytitanium and its Reactivity to Carbonyl Compounds(1996)
- A Study on the Synthesis of 2-Thiophenyltriisopropoxytitanium and its Reactivity to Carbonyl Compounds(1994)