Visible light induced redox neutral fragmentation of 1,2-diol derivatives

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Abstract

A homogeneous, redox-neutral photo fragmentation of diol derivatives was developed. Under photo/hydrogen atom transfer (HAT) dual catalysis, diol derivatives such as lignin model compounds and diol monoesters undergo selective β C(sp3)-O bond cleavage to afford ketones, phenols and acids effectively.

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Chen, K., Schwarz, J., Karl, T. A., Chatterjee, A., & König, B. (2019). Visible light induced redox neutral fragmentation of 1,2-diol derivatives. Chemical Communications, 55(87), 13144–13147. https://doi.org/10.1039/c9cc06904f

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