articleTop 1% cited
Oxone as an Inexpensive, Safe, and Environmentally Benign Oxidant for C−H Bond Oxygenation
Organic Letters · 2006 · Vol. 8(6) · pp. 1141–1144
Lopa V. Desai✉(University of Michigan–Ann Arbor)Hasnain A. Malik(University of Michigan–Ann Arbor)Melanie S. Sanford(University of Michigan–Ann Arbor)
Abstract
[reaction: see text] This paper describes the application of peroxide-based oxidants in the Pd(OAc)(2)-catalyzed acetoxylation and etherification of arene and alkane C-H bonds. Oxone in acetic acid and/or methanol proved particularly effective, and these transformations were applied to a wide variety of substrates.
Oxidative Organic Chemistry ReactionsCatalytic C–H Functionalization MethodsSynthesis and Catalytic ReactionsChemistryMethanolAcetic acidAlkaneCatalysisPeroxideCombinatorial chemistryOrganic chemistryOxygenationHydrogen peroxide
MeSH terms
Indicators and ReagentsPeroxidesSulfuric AcidsMolecular StructureOxidantsCombinatorial Chemistry Techniques
Citations
421
FWCI
11.66
field-weighted impact
References
16
Percentile
99%
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