Reductive Cleavage of Azoarene as a Key Step in Nickel-Catalyzed Amidation of Esters with Nitroarenes-Reference-Cited by-同舟云学术

Reductive Cleavage of Azoarene as a Key Step in Nickel-Catalyzed Amidation of Esters with Nitroarenes

Published:2020-01-21 Issue:4 Volume:10 Page:2845-2854
ISSN:2155-5435
Container-title:ACS Catalysis
language:en
Short-container-title:ACS Catal.

Author:

Ploeger Marten L.¹,Darù Andrea²^ORCID,Harvey Jeremy N.²^ORCID,Hu Xile¹^ORCID

Affiliation:

1. Laboratory of Inorganic Synthesis and Catalysis, Institute of Chemical Sciences and Engineering, École Polytechnique Fédérale de Lausanne (EPFL), ISIC-LSCI, BCH 3305, Lausanne 1015, Switzerland

2. Department of Chemistry, KU Leuven, Celestijnenlaan 200F, B-3001 Leuven, Belgium

Funder

H2020 Marie Sklodowska-Curie Actions

Publisher

American Chemical Society (ACS)

Subject

Catalysis,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acscatal.9b05049

Reference43 articles.

1. Ono, N. The Nitro Group in Organic Synthesis; Wiley-VCH: New York, 2001; pp 302–321.

2. The Suzuki–Miyaura Coupling of Nitroarenes

3. Nucleophilic displacement of aromatic nitro groups

4. Ligand-free copper-catalyzed coupling of nitroarenes with arylboronic acids

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