Palladium-Catalyzed Reductive Aminocarbonylation of Benzylammonium Triflates with o-Nitrobenzaldehydes for the Synthesis of 3-Arylquinolin-2(1H)-ones-Reference-Cited by-同舟云学术

Palladium-Catalyzed Reductive Aminocarbonylation of Benzylammonium Triflates with o-Nitrobenzaldehydes for the Synthesis of 3-Arylquinolin-2(1H)-ones

Published:2021-09-20 Issue:19 Volume:86 Page:13824-13832
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Liu Yongzhu¹,Qi Xinxin¹,Wu Xiao-Feng²^ORCID

Affiliation:

1. Department of Chemistry, Key Laboratory of Surface & Interface Science of Polymer Materials of Zhejiang Province, Zhejiang Sci-Tech University, Hangzhou 310018, China

2. Dalian National Laboratory for Clean Energy, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, Liaoning 116023, China

Funder

Zhejiang Sci-Tech University

Natural Science Foundation of Zhejiang Province

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.1c01984

Reference63 articles.

1. Natural product chemistry. Part 116. Synthesis of daurine and folidine: Two 2(1H)-quinolinone alkaloids fromHaplophyllum species

2. 3-Phenyl-4-hydroxyquinolin-2(1H)-ones: potent and selective antagonists at the strychnine-insensitive glycine site on the N-methyl-D-aspartate receptor complex

3. Quinoline, quinazoline, and acridone alkaloids

4. 4-Substituted-3-phenylquinolin-2(1H)-ones: Acidic and Nonacidic Glycine Site N-Methyl-d-aspartate Antagonists with in Vivo Activity

5. Implications for selectivity of 3,4-diarylquinolinones as p38αMAP kinase inhibitors

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