Synthesis and Mechanistic Investigation of Bipyrazolo[1,5-a]pyridines via Palladium-Catalyzed Cross-Dehydrogenative Coupling of Pyrazolo[1,5-a]pyridines-Reference-Cited by-同舟云学术

Synthesis and Mechanistic Investigation of Bipyrazolo[1,5-a]pyridines via Palladium-Catalyzed Cross-Dehydrogenative Coupling of Pyrazolo[1,5-a]pyridines

Published:2022-07-18 Issue:15 Volume:87 Page:9851-9863
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Hsiao Pu-Yen¹,Chang Rong²,Sue Andrew C.-H.²^ORCID,Chu Jean-Ho¹^ORCID,Liao Guan-Wei¹,Lee Yi-Hsin¹,Huang Jui-Yang¹

Affiliation:

1. Department of Applied Science, National Taitung University, Taitung 95092, Taiwan, R.O.C.

2. College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, China

Funder

Ministry of Science and Technology, Taiwan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.2c00895

Reference64 articles.

1. The compound TB47 is highly bactericidal against Mycobacterium ulcerans in a Buruli ulcer mouse model

2. Identification of Pyrazolo[1,5-a]pyridine-3-carboxamide Diaryl Derivatives as Drug Resistant Antituberculosis Agents

3. Design, Synthesis, and Biological Evaluation of Pyrazolo[1,5-a]pyridine-3-carboxamides as Novel Antitubercular Agents

4. Discovery of Pyridazinone and Pyrazolo[1,5-a]pyridine Inhibitors of C-Terminal Src Kinase

5. Pyrazolo[1,5-a]pyridine Inhibitor of the Respiratory Cytochrome bcc Complex for the Treatment of Drug-Resistant Tuberculosis

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