Metal-free oxidative cross-dehydrogenative coupling of quinones with benzylic C(sp3)-H bonds

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Abstract

A metal-free cross-dehydrogenative coupling of quinones with toluene derivatives has been established. A series of quinones were subjected to reaction with toluene derivatives in the presence of di-tertbutyl peroxide (DTBP) for direct synthesis of benzylquinones. The method exhibits good functional group tolerance, and desired products were obtained in moderate to good yields. Meanwhile, a radical pathway was proposed to describe the cross-dehydrogenative coupling of quinones with toluene derivatives.

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Dong, Y., Yang, J., He, S., Shi, Z. C., Wang, Y., Zhang, X. M., & Wang, J. Y. (2019). Metal-free oxidative cross-dehydrogenative coupling of quinones with benzylic C(sp3)-H bonds. RSC Advances, 9(47), 27588–27592. https://doi.org/10.1039/c9ra05678e

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