Issue 6, 2019

Nickel-promoted C(2)–H amidation of quinoline N-oxides with N-fluorobenzenesulfonimide

Abstract

Reported herein is an unprecedented nickel-promoted C–H amidation reaction of quinoline N-oxides using N-fluorobenzenesulfonimide (NFSI) as the amination reagent. This strategy provides a convenient access to a variety of useful 1,2-dihydro-2-iminoquinolines in moderate to good yields. Notable advantages of this protocol include easy operation and mild reaction conditions.

Graphical abstract: Nickel-promoted C(2)–H amidation of quinoline N-oxides with N-fluorobenzenesulfonimide

Supplementary files

Article information

Article type
Research Article
Submitted
27 Nov 2018
Accepted
01 Feb 2019
First published
05 Feb 2019

Org. Chem. Front., 2019,6, 830-834

Nickel-promoted C(2)–H amidation of quinoline N-oxides with N-fluorobenzenesulfonimide

S. Han, X. Gao, Q. Wu, J. Li, D. Zou, Y. Wu and Y. Wu, Org. Chem. Front., 2019, 6, 830 DOI: 10.1039/C8QO01281D

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