
Bulletin of the Chemical Society of Japan p. 3479 - 3481 (1991)
Update date:2022-09-26
Topics:
Kamigata, Nobumasa
Ishii, Kimiko
Ohtsuka, Takeshi
Matsuyama, Haruo
In the presence of a catalytic amount of dichlorotris(triphenylphosphine)ruthenium(II), the reactions of arenesulfonyl chlorides with allyl phenyl sulfide and allyl phenyl selenide proceeded smoothly to give allyl phenyl sulfone in high yield as well as the corresponding diphenyl disulfide or diphenyl diselenide.An SH2'-type mechanism involving the arenesulfonyl radical is proposed.
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