Manganese-mediated reductive amidation of esters with nitroarenes-Reference-Cited by-同舟云学术

Manganese-mediated reductive amidation of esters with nitroarenes

Published:2019 Issue:6 Volume:6 Page:756-761
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Cheung Chi Wai¹²³⁴⁵^ORCID,Shen Ni¹²³⁴⁵,Wang Shao-Peng¹²³⁴⁵,Ullah Asim¹²³⁴⁵,Hu Xile⁶⁷⁸⁹¹⁰^ORCID,Ma Jun-An¹²³⁴⁵^ORCID

Affiliation:

1. Department of Chemistry

2. Tianjin Key Laboratory of Molecular Optoelectronic Sciences

3. and Tianjin Collaborative Innovation Center of Chemical Science & Engineering

4. Tianjin University

5. Tianjin 300072

6. Laboratory of Inorganic Synthesis and Catalysis

7. Institute of Chemical Sciences and Engineering

8. Ecole Polytechnique Fédérale de Lausanne (EPFL)

9. Lausanne 1015

10. Switzerland

Abstract

N-Aryl amides were synthesized via the manganese-mediated amidation of esters with nitroarenes without the need for additional catalysts or ligands.

Funder

National Natural Science Foundation of China

Tianjin University

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/QO/C8QO01405A

Reference53 articles.

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2. A. Greenberg , C. M.Breneman and J. F.Liebman , The Amide Linkage: Structural Significance in Chemistry, Biochemistry, and Materials Science , Wiley-Interscience , New York , 2000

3. Chemical Synthesis of Natural Product Peptides: Coupling Methods for the Incorporation of Noncoded Amino Acids into Peptides

4. Metal-catalysed approaches to amide bond formation

5. Metal-catalyzed amidation

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