Further functional group oxidations using sodium perborate
Alexander McKillop* and Duncan Kemp
*School of Chemical Sciences, University of East Anglia, Norwich, NR4 7TJ, England
A. McKillop, D. Kemp, Tetrahedron, 1989, 45, 3299-3306.
DOI: 10.1016/S0040-4020(01)81008-5
see article for more examples
see article for more examples
Abstract
Sodium perborate in acetic acid is an effective reagent for the oxidation of aromatic aldehydes to carboxylic acids, iodoarenes to (diacetoxyiodo)arenes, azines to N-oxides, and various sulphur heterocycles to S,S-dioxides. Nitriles undergo smooth oxidative hydration to amides when aqueous methanol is employed as solvent.
see article for more examples
see article for more reactions
see article for more examples
Key Words
Carboxylic Acids, Hypervalent Iodine(III) Compounds, N-Oxides, Amides, Sodium Perborate
ID: J72-Y1989-060