NHC-Catalyzed Enantioselective [3 + 3] Annulation to Construct 5,6-Dihydropyrimidin-4-ones-Reference-Cited by-同舟云学术

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NHC-Catalyzed Enantioselective [3 + 3] Annulation to Construct 5,6-Dihydropyrimidin-4-ones

Published:2020-09-23 Issue:19 Volume:22 Page:7635-7639
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Meng Di¹²,Xie Yangxi³,Peng Qiupeng³,Wang Jian¹³^ORCID

Affiliation:

1. School of Biotechnology and Health Sciences, Jiangmen International Healthcare Innovation Institute, Wuyi University, Jiangmen 529020, China

2. School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou 510006, China

3. School of Pharmaceutical Sciences, Tsinghua University, Beijing 100084, China

Funder

Bayer

Ministry of Science and Technology of the People's Republic of China

Tsinghua University

Ministry of Human Resources and Social Security

National Natural Science Foundation of China

Central Committee of the Communist Party of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.0c02832

Reference53 articles.

1. Biologically active dihydropyrimidones of the Biginelli-type — a literature survey

2. Recent synthetic and medicinal perspectives of dihydropyrimidinones: A review

3. Biological activity of dihydropyrimidinone (DHPM) derivatives: A systematic review

4. Dihydropyrimidine calcium channel blockers. 3. 3-Carbamoyl-4-aryl-1,2,3,4-tetrahydro-6-methyl-5-pyrimidinecarboxylic acid esters as orally effective antihypertensive agents

5. Dihydropyrimidine calcium channel blockers. 4. Basic 3-substituted-4-aryl-1,4-dihydropyrimidine-5-carboxylic acid esters. Potent antihypertensive agents

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