Issue 87, 2019

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

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.

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

Supplementary files

Article information

Article type
Communication
Submitted
04 Sep 2019
Accepted
07 Oct 2019
First published
07 Oct 2019

Chem. Commun., 2019,55, 13144-13147

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

K. Chen, J. Schwarz, T. A. Karl, A. Chatterjee and B. König, Chem. Commun., 2019, 55, 13144 DOI: 10.1039/C9CC06904F

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