Alternative reagent with enhanced stability for many of the reactions conventionally carried out using 3-Chloroperoxybenzoic acid, L00286. For a comparative study of the two reagents, see: Synthesis, 1015 (1987)./n
For regioselective epoxidation of allylic alcohols in water, see: J. Org. Chem., 57, 1198 (1992)./n
Cyclic ketones undergo the Baeyer-Villiger reaction to give lactones in high yield, in acetonitrile: Synth. Commun., 26, 4591 (1996), or in methanol-water in the presence of NaHCO3: J. Org. Chem., 62, 2633 (1997); the latter method has been used in the synthesis of massoia lactone./n
Mentions de danger (UE): H315-H319-H335
Causes skin irritation. Causes serious eye irritation. May cause respiratory irritation.
Mentions de prudence: P261-P280a-P305+P351+P338-P304+P340-P405-P501a
Avoid breathing dust/fume/gas/mist/vapours/spray. Wear protective gloves and eye/face protection. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.