Diversity-Oriented Synthesis of Spiro[chromeno[2,3-<i>b</i>]pyridine-3,4′-pyrazole] Derivatives via Pseudo-Three-Component Reactions-Reference-Cited by-同舟云学术

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Diversity-Oriented Synthesis of Spiro[chromeno[2,3-b]pyridine-3,4′-pyrazole] Derivatives via Pseudo-Three-Component Reactions

Published:2024-07-09 Issue:14 Volume:89 Page:10371-10378
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Zhou Wenyan¹,Lv Jiaman¹,Wang Cunde¹^ORCID

Affiliation:

1. School of Chemistry and Chemical Engineering, Yangzhou University, 180 Siwangting Street, Yangzhou 225002, P. R. China

Funder

Priority Academic Program Development of Jiangsu Higher Education Institutions

Top-notch Academic Programs Project of Jiangsu Higher Education Institutions

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.4c00959

Reference44 articles.

1. Catalytic Asymmetric Synthesis of Spiropyrazolones and their Application in Medicinal Chemistry

2. Asymmetric synthesis of pyrazoles and pyrazolones employing the reactivity of pyrazolin-5-one derivatives

3. Discovery of pyrazolone spirocyclohexadienone derivatives with potent antitumor activity

4. New development in the enantioselective synthesis of spiro compounds

5. Novel spiropyrazolone antitumor scaffold with potent activity: Design, synthesis and structure–activity relationship

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