Journal of the Chemical Society. Chemical communications p. 1501 - 1502 (1983)
Update date:2022-08-04
Topics:
Uemura, Sakae
Fukuzawa, Shin-ichi
Toshimitsu, Akio
Oxidation of alkyl phenyl selenides with m-chloroperbenzoic acid in methanol at room temperature affords the corresponding alkyl methyl ethers almost quantitatively, the reaction being accompanied by phenyl migration and ring-contraction respectively when applied to selenides having a phenyl group vicinal to the phenylselenium moiety and to some methoxyselenation products of cyclic olefins.
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