Enantioselective Formation of All-Carbon Quaternary Stereocenters in gem-Difluorinated Cyclopropanes via Rhodium-Catalyzed Stereoablative Kinetic Resolution
Author:
Affiliation:
1. West China School of Public Health and West China Fourth Hospital, West China-PUMC C.C. Chen Institute of Health, and State Key Laboratory of Biotherapy, Sichuan University, Chengdu 610041, China
Funder
Sichuan University
National Natural Science Foundation of China
Thousand Young Talents Program 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.2c02410
Reference54 articles.
1. Recent Developments in Cyclopropane Cycloaddition Reactions
2. Creating Stereocenters within Acyclic Systems by C–C Bond Cleavage of Cyclopropanes
3. Catalytic Enantioselective Ring-Opening Reactions of Cyclopropanes
4. Visible‐Light‐Mediated Ring‐Opening Reactions of Cyclopropanes
5. The “Cyclopropyl Fragment” is a Versatile Player that Frequently Appears in Preclinical/Clinical Drug Molecules
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