Sulfuration‐Triggered Radical Cyclization of o ‐Cyanoarylacrylamides to 3‐Thiomethylated Quinoline‐2,4‐dione-Reference-Cited by-同舟云学术

Sulfuration‐Triggered Radical Cyclization of o ‐Cyanoarylacrylamides to 3‐Thiomethylated Quinoline‐2,4‐dione

Published:2020-12-08 Issue:46 Volume:5 Page:14534-14537
ISSN:2365-6549
Container-title:ChemistrySelect
language:en
Short-container-title:ChemistrySelect

Author:

Yin Zizhen¹,Yu Yingjie¹,Li Chunxiang²,Mei Haibo¹,Zhu Kai¹,Han Jianlin¹^ORCID

Affiliation:

1. Jiangsu Co–Innovation Center of Efficient Processing and Utilization of Forest Resources College of Chemical Engineering Nanjing Forestry University Nanjing 210037 China

2. Shandong Key Laboratory of Biochemical Analysis College of Chemistry and Molecular Engineering Qingdao University of Science and Technology Qingdao 266042 PR China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/slct.202003999

Reference36 articles.

2. HIV Inhibitory Natural Products. 26. Quinoline Alkaloids from Euodia roxburghiana

3. Discovery of 3-aryl-3-methyl-1H-quinoline-2,4-diones as a new class of selective 5-HT6 receptor antagonists

4. Synthesis and anti-HIV activity of alkylated quinoline 2,4-diols

5. Development of Quinoline-2,4(1H,3H)-diones as Potent and Selective Ligands of the Cannabinoid Type 2 Receptor

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