Journal of the Chemical Society. Chemical communications p. 425 - 426 (1981)
Update date:2022-08-03
Topics:
Fujita, Shinsaku
In the solvolysis of 4-alkoxy-5-methyl-o-benzoquinone N-arylsulphonylimines (1a) and (1b) (NaOH-MeOH-H2O), the regiospecific attack of MeO- occurs initially on the carbon atom substituted by the alkoxy-group to produce the p-benzoquinone monoacetals (3a)
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