Abstract
A general and efficient aerobic oxidation of N-substituted hydroxylamines is described. The mild reaction conditions employed provide a catalytic and sustainable alternative to stoichiometric oxidation methods to gain access to a range of nitroso compounds, such as acylnitroso, nitrosoformate, nitrosoformamide, iminonitroso, arylnitroso, and P-nitrosophosphine oxide derivatives in excellent yield. © 2012 American Chemical Society.
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CITATION STYLE
Frazier, C. P., Bugarin, A., Engelking, J. R., & Read De Alaniz, J. (2012). Copper-catalyzed aerobic oxidation of N-substituted hydroxylamines: Efficient and practical access to nitroso compounds. Organic Letters, 14(14), 3620–3623. https://doi.org/10.1021/ol301414k
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