Amide synthesis via nickel-catalysed reductive aminocarbonylation of aryl halides with nitroarenes-Reference-Cited by-同舟云学术

Amide synthesis via nickel-catalysed reductive aminocarbonylation of aryl halides with nitroarenes

Published:2018 Issue:3 Volume:9 Page:655-659
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Cheung Chi Wai¹²³⁴⁵,Leendert Ploeger Marten¹²³⁴⁵,Hu Xile¹²³⁴⁵^ORCID

Affiliation:

1. Laboratory of Inorganic Synthesis and Catalysis

2. Institute of Chemical Sciences and Engineering

3. Ecole Polytechnique Fédérale de Lausanne (EPFL)

4. ISIC-LSCI

5. Lausanne 1015

Abstract

A nickel-catalysed reductive aminocarbonylation of (hetero)aryl halides employing readily available nitro(hetero)arenes as the nitrogen source has been developed.

Funder

École Polytechnique Fédérale de Lausanne

H2020 Marie Skłodowska-Curie Actions

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/SC/C7SC03950F

Reference38 articles.

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2. Metal-catalyzed amidation

3. Rethinking amide bond synthesis

4. Nonclassical Routes for Amide Bond Formation

5. Large-Scale Applications of Amide Coupling Reagents for the Synthesis of Pharmaceuticals

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