Journal of the Chemical Society. Chemical communications p. 426 - 427 (1984)
Update date:2022-09-26
Topics:
Uemura, Sakae
Fukuzawa, Shin-ichi
Yamauchi, Takayoshi
Hattori, Kaneaki
Mizutaki, Shoichi
Tamaki, Kentaro
Oxidation with m-chloroperbenzoic acid of the ethylene acetals of aryl α-phenylseleno- or aryl α-phenyltelluro-ethyl ketones prepared by treating the corresponding α-bromo compounds with diphenyl diselenide-sodium or diphenyl ditelluride-sodium, respectively, affords hydroxyethyl 2-arylpropanoates in moderate to good yields via aryl group migration.
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