Visible light-induced direct α C–H functionalization of alcohols

153Citations
Citations of this article
78Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Considering the synthetic value of introducing active alcoholic hydroxyl group, developing C–H functionalization of alcohols is of significance. Herein, we present a photochemical method that under visible light irradiation, selectfluor can effectively promote the oxidative cross-coupling between alcohols and heteroarenes without the external photocatalysis, achieving the selective α sp 3 C–H arylation of alcohol, even in the presence of ether. The N-F activation of selectfluor under blue LEDs irradiation is evidenced by electron paramagnetic resonance (EPR) study, which is the key process for the oxidative activation of α sp 3 C–H alcohols. The observed reactivity may have significant implications for chemical transformations.

Cite

CITATION STYLE

APA

Niu, L., Liu, J., Liang, X. A., Wang, S., & Lei, A. (2019). Visible light-induced direct α C–H functionalization of alcohols. Nature Communications, 10(1). https://doi.org/10.1038/s41467-019-08413-9

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free