Journal of the Chemical Society. Chemical communications p. 2319 - 2320 (1995)
Update date:2022-08-17
Topics:
Akai, Shuji
Iio, Kiyosei
Takeda, Yoshifumi
Ueno, Hiroshi
Yokogawa, Kayoko
Kita, Yasuyuki
The treatment of p-(phenylsulfinyl)phenyl ethers 1 with trifluoroacetic anhydride in the presence of styrene selectively caused the direct ipso-substitution of the sulfinyl groups by trifluoroacetoxy groups, giving the protected dihydroquinone derivatives 3 in high to quantitative yields.
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