Manganese-mediated reductive amidation of esters with nitroarenes

文献信息

发布日期 2019-01-30

DOI 10.1039/C8QO01405A

影响因子 5.281

作者

Chi Wai Cheung, Ni Shen, Shao-Peng Wang, Asim Ullah, Xile Hu, Jun-An Ma

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摘要

Amides are ubiquitous molecules in nature and in synthetic chemistry. Here we report a convenient and efficient method to synthesize N-aryl amides via amidation of esters with nitroarenes. In the presence of manganese metal, this amidation proceeded smoothly without the need for additional catalysts or ligands. Various esters and nitroarenes are suitable substrates to afford a wide range of N-aryl amides, including bio-active molecules and intermediates to drug molecules.

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Bio-Medical Materials and Engineering

Composite Interfaces

Synlett

Current Medicinal Chemistry

Computational Materials Science

Advanced Materials

Cement and Concrete Composites

Applied Composite Materials

Catalysis Today

Construction and Building Materials

来源期刊

Organic Chemistry Frontiers

CiteScore: 7.8

自引率: 8.7%

年发文量: 724

Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry

Manganese-mediated reductive amidation of esters with nitroarenes

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