Diastereoselective Synthesis of 4-Hydroxy-2-quinolinones via Formal [2 + 4] Cycloaddition Reactions Using α-Diazo Pyrazoleamides as C2 Synthons-Reference-Cited by-同舟云学术

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Diastereoselective Synthesis of 4-Hydroxy-2-quinolinones via Formal [2 + 4] Cycloaddition Reactions Using α-Diazo Pyrazoleamides as C2 Synthons

Published:2024-06-24 Issue:26 Volume:26 Page:5554-5559
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Li Pei¹,Shi Maoqing¹,Yang Kaixin¹,Jing Tongfei²,Kang Zhenghui²,Hu Wenhao¹^ORCID,Qian Yu¹^ORCID

Affiliation:

1. State Key Laboratory of Anti-Infective Drug Discovery and Development, Guangdong Provincial Key Laboratory of Chiral Molecule and Drug Discovery, School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China

2. Zhongshan Institute for Drug Discovery, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Zhongshan 528400, China

Funder

Guangdong Provincial Department of Science and Technology

China Postdoctoral Science Foundation

National Natural Science Foundation of China

Natural Science Foundation of Guangdong Province

Guangdong Provincial Key Laboratory of Chiral Molecule and Drug Discovery, Sun Yat-Sen University

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.4c01956

Reference53 articles.

1. The effects of adding quinolones to beta‐lactam antibiotics for sepsis

2. Quinolone antibiotics

3. The 3,4-dioxygenated 5-hydroxy-4-aryl-quinolin-2(1H)-one alkaloids. Results of 20 years of research, uncovering a new family of natural products

4. A review on anticancer potential of bioactive heterocycle quinoline

5. Mechanism of Quinolone Action and Resistance

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