Theoretical investigation on the mechanism of Cu(ii)-catalyzed synthesis of 4-quinolones: effects of additives HOTf vs. HOTs-Reference-Cited by-同舟云学术

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Theoretical investigation on the mechanism of Cu(ii)-catalyzed synthesis of 4-quinolones: effects of additives HOTf vs. HOTs

Published:2019 Issue:10 Volume:43 Page:4291-4305
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Yuan Binfang¹²³⁴⁵^ORCID,Guo Xiaogang¹²³⁴⁵,Wang Guangzhao⁶⁷³⁴⁵,Huang Huisheng¹²³⁴⁵,Zhang Fulan¹²³⁴⁵,Xu Jianhua¹²³⁴⁵,He Rongxing²⁸⁹⁵^ORCID

Affiliation:

1. Chongqing Key Laboratory of Inorganic Special Functional Materials

2. College of Chemistry and Chemical Engineering

3. Yangtze Normal University

4. Chongqing 408100

5. China

6. College of Electronic Information Engineering

7. Key Laboratory of Extraordinary Bond Engineering and Advanced Materials, Technology

8. Southwest University

9. Chongqing 400715

Abstract

Hydrogen-bond donor/proton-donor ability is revealed to be the primary factor that controls the catalytic capability of additives (HOTf vs. HOTs).

Funder

National Natural Science Foundation of China

Chongqing Municipal Education Commission Foundation

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2019/NJ/C9NJ00082H

Reference69 articles.

1. Discovery and Characterization of (8S,9R)-5-Fluoro-8-(4-fluorophenyl)-9-(1-methyl-1H-1,2,4-triazol-5-yl)-2,7,8,9-tetrahydro-3H-pyrido[4,3,2-de]phthalazin-3-one (BMN 673, Talazoparib), a Novel, Highly Potent, and Orally Efficacious Poly(ADP-ribose) Polymerase-1/2 Inhibitor, as an Anticancer Agent

2. Development of Novel 1,2,3,4-Tetrahydroquinoline Scaffolds as Potent NF-κB Inhibitors and Cytotoxic Agents

3. Structure–Activity Relationship Studies with Tetrahydroquinoline Analogs as EPAC Inhibitors

4. 4-Quinolone derivatives and their activities against Gram positive pathogens

5. Synthesis, antibacterial properties and 2D-QSAR studies of quinolone-triazole conjugates

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