Issue 23, 2018

Copper mediated C–H amination with oximes: en route to primary anilines

Abstract

Here we report an efficient Cu(I)-mediated C–H amination reaction with oximes as amino donors to introduce NH2 groups directly. Various strongly coordinating heterocycles including quinoline, pyrimidine, pyrazine, pyrazole and triazole were tolerated well. The potential utility was further demonstrated in a late-stage modification of telmisartan (an antagonist for the angiotensin II receptor).

Graphical abstract: Copper mediated C–H amination with oximes: en route to primary anilines

Supplementary files

Article information

Article type
Edge Article
Submitted
17 Mar 2018
Accepted
12 May 2018
First published
14 May 2018
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY-NC license

Chem. Sci., 2018,9, 5160-5164

Copper mediated C–H amination with oximes: en route to primary anilines

L. Xu, X. Wang, B. Ma, M. Yin, H. Lin, H. Dai and J. Yu, Chem. Sci., 2018, 9, 5160 DOI: 10.1039/C8SC01256C

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