American Chemical Society
Browse
ol5b03705_si_001.pdf (17.38 MB)

Visible Light Photoredox Cross-Coupling of Acyl Chlorides with Potassium Alkoxy­methyl­trifluoro­borates: Synthesis of α‑Alkoxyketones

Download (17.38 MB)
journal contribution
posted on 2016-02-01, 00:00 authored by Javad Amani, Esmat Sodagar, Gary A. Molander
A visible-light, single-electron-transfer (SET), photoredox cross-coupling for the synthesis of α-alkoxyketones has been developed. In this method, various aliphatic and aromatic acyl chlorides were successfully coupled with structurally diverse potassium alkoxy­methyl­trifluoro­borates, producing the corresponding α-alkoxyketones with high yields. In this operationally simple and mild cross-coupling protocol, the desired ketones are obtained in one step from bench stable starting materials by a bond connection that is unique to both alkylboron chemistry and photoredox/Ni catalysis.

History