Nickel-catalyzed reductive monofluoroakylation of alkyl tosylate with bromofluoromethane to primary alkyl fluoride.

Chem Commun (Camb)

Hefei National Laboratory for Physical Sciences at the Microscale and Department of Chemistry, University of Science and Technology of China, Hefei, Anhui 230026, P. R. China.

Published: September 2021

A nickel-catalysed direct terminal monofluoromethlyation between alkyl tosylates and a low-cost, industrial raw material bromofluoromethane has been developed. This transformation has demonstrated high efficiency, mild conditions, and good functional-group compatibility. The key to success of this transformation lies in the ligand and mild base selection, ensuring the generation of various terminal monofluormethylation products.

Download full-text PDF

Source
http://dx.doi.org/10.1039/d1cc02837eDOI Listing

Publication Analysis

Top Keywords

nickel-catalyzed reductive
4
reductive monofluoroakylation
4
monofluoroakylation alkyl
4
alkyl tosylate
4
tosylate bromofluoromethane
4
bromofluoromethane primary
4
primary alkyl
4
alkyl fluoride
4
fluoride nickel-catalysed
4
nickel-catalysed direct
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!