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.
Cite
CITATION STYLE
APA
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
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.
Already have an account? Sign in
Sign up for free