Direct Synthesis of α-Ketoamides via Copper-Catalyzed Reductive Amidation of Nitroarenes with α-Oxocarboxylic Acids-Reference-Cited by-同舟云学术

Direct Synthesis of α-Ketoamides via Copper-Catalyzed Reductive Amidation of Nitroarenes with α-Oxocarboxylic Acids

Published:2024-04-24 Issue:9 Volume:89 Page:6575-6583
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Liu Jialing¹,Yao Jiaxin¹,Du Jiahui¹,Yu Lin¹^ORCID,Duan Wengui¹^ORCID,Xiao Yuxuan¹,Lei Zhiguo¹

Affiliation:

1. School of Chemistry and Chemical Engineering, Guangxi Colleges and Universities Key Laboratory of Applied Chemistry Technology and Resource Development, Guangxi University, Nanning, Guangxi 530004, P. R. China

Funder

Guangxi University

Specific Research Project of Guangxi for Research Bases and Talents

Natural Science Foundation of Guangxi Zhuang Autonomous Region

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.4c00237

Reference68 articles.

1. Cyclotheonamide E4 and E5, New Potent Tryptase Inhibitors from an Ircinia Species of Sponge

2. Three more cyclotheonamides, C, D, and E, potent thrombin inhibitors from the marine sponge Theonella swinhoei

3. Synthesis of DEFG Ring of Complestatin and Chloropeptin I: Highly Atropdiastereoselective Macrocyclization by Intramolecular Suzuki-Miyaura Reaction

4. Synthesis of Diastereomers of Complestatin and Chloropeptin I: Substrate-Dependent Atropstereoselectivity of the Intramolecular Suzuki–Miyaura Reaction

5. Recent Developments in General Methodologies for the Synthesis of α-Ketoamides

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