Asymmetric Hydrogenation of Tetrasubstituted α,β-Unsaturated Ketones: Access to Chiral 2-Substituted Cyclopentyl Aryl Ketones-Reference-Cited by-同舟云学术

Asymmetric Hydrogenation of Tetrasubstituted α,β-Unsaturated Ketones: Access to Chiral 2-Substituted Cyclopentyl Aryl Ketones

Published:2023-02-10 Issue:3 Volume:1 Page:146-152
ISSN:2771-9316
Container-title:Precision Chemistry
language:en
Short-container-title:Precision Chemistry

Author:

Ding Zhengdong¹²,Gao Feng¹,Lu Yining¹,Yuan Qianjia¹,Deng Wei-Ping²³^ORCID,Zhang Wanbin¹^ORCID

Affiliation:

1. Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs, Frontiers Science Center for Transformative Molecules, School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai 200240, China

2. Shanghai Key Laboratory of New Drug Design, School of Pharmacy, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, China

3. Key Laboratory of the Ministry of Education for Advanced Catalysis Materials, Department of Chemistry, Zhejiang Normal University, 688 Yingbin Road, Jinhua 321004, China

Funder

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

Science and Technology Commission of Shanghai Municipality

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/prechem.2c00010

Reference55 articles.

1. Design and Synthesis of a Novel Series of 1,2-Disubstituted Cyclopentanes as Small, Potent Potentiators of 2-Amino-3-(3-hydroxy-5-methyl-isoxazol-4-yl)propanoic Acid (AMPA) Receptors

2. Highly Substituted Cyclopentane–CMP Conjugates as Potent Sialyltransferase Inhibitors

3. Navigating the Chiral Pool in the Total Synthesis of Complex Terpene Natural Products