A Tandem Regiospecific [3 + 2] Annulation/Ring Cleavage Reaction for the Synthesis of β-Ketoenamides-Reference-Cited by-同舟云学术

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A Tandem Regiospecific [3 + 2] Annulation/Ring Cleavage Reaction for the Synthesis of β-Ketoenamides

Published:2024-01-31 Issue:4 Volume:89 Page:2800-2806
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Dong Jun¹^ORCID,Zhang Tuojiang¹,Chen Youwei¹,Sheng Chengcai¹,Wang Yanqing¹,Zhang Xuehua¹

Affiliation:

1. School of Chemistry and Environmental Engineering, Yancheng Teachers University, Yancheng City 224007, People’s Republic of China

Funder

Natural Science Research of Jiangsu Higher Education Institutions of China

Qinglan Project of Jiangsu Province of China

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.3c02717

Reference30 articles.

1. Solid-State Synthesis of β-Enamino Ketones from Solid 1,3-Dicarbonyl Compounds and Ammonium Salts or Amines

2. Gold catalysis in the reactions of 1,3-dicarbonyls with nucleophiles

3. Selective Dehydrogenative Acylation of Enamides with Aldehydes Leading to Valuable β-Ketoenamides

4. Copper-Catalyzed Reductive Ring-Cleavage of Isoxazoles: Synthesis of Fluoroalkylated Enaminones and Application for the Preparation of Celecoxib, Deracoxib, and Mavacoxib

5. Iron-Catalyzed Transfer Hydrogenation in Aged N-Methyl-2-pyrrolidone: Reductive Ring-Opening of 3,5-Disubstituted Isoxazoles and Isoxazolines

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