Issue 72, 2021

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

Abstract

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.

Graphical abstract: Nickel-catalyzed reductive monofluoroakylation of alkyl tosylate with bromofluoromethane to primary alkyl fluoride

Supplementary files

Article information

Article type
Communication
Submitted
01 Jun 2021
Accepted
10 Aug 2021
First published
11 Aug 2021

Chem. Commun., 2021,57, 9084-9087

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

R. Cui, J. Sheng, B. Wu, D. Hu, H. Zheng and X. Wang, Chem. Commun., 2021, 57, 9084 DOI: 10.1039/D1CC02837E

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