Abstract

AbstractA one-pot, three-component difunctionalization of quinones with indoles and arylamines has been developed to synthesize indole functionalized p-iminoquinones derivatives. The approach employed AgOAc as the catalyst in the presence of 3-chlorophenylboronic acid, giving a series of indole functionalized p-iminoquinones derivatives in moderate to good yields. This catalytic approach represents a step-economic and convenient strategy for the difunctionalization of quinones. A plausible reaction pathway has been proposed based on a series of control experiments.

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