Journal of the Chemical Society. Perkin transactions I p. 1473 - 1476 (1981)
Update date:2022-08-05
Topics:
Barton, Derek H. R.
Brewster, Andrew G.
Ley, Steven V.
Read, Christine M.
Rosenfeld, Moshe N.
Benzeneseleninic anhydride has been used as a mild oxidising reagent to convert phenols into o-quinones including some examples where the p-position is unblocked.The method is limited to the production of o-quinones which are not susceptible to futher reaction.Pyrocatechols and hydroquinones can also be oxidised to the corresponding quinones in excellent yield using benzeneseleninic anhydride.
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Doi:10.1021/jo00335a038
(1981)Doi:10.1007/BF00503334
(1981)Doi:10.1080/10426509708040491
(1997)Doi:10.1007/BF00950308
(1981)Doi:10.1021/jacs.5b00728
(2015)Doi:10.1016/S0022-328X(00)83994-7
(1981)
