Palladium/Amino Acid Co-catalyzed Atroposelective C–H Olefination to Access Tetra-Ortho-Substituted Atropisomers Featuring 2,2′-Difluoro-1-biaryl Scaffolds
Author:
Affiliation:
1. College of Chemistry and Chemical Engineering, Qingdao University, Qingdao 266071, China
Funder
Taishan Scholar Foundation of Shandong Province
Qingdao University
National Natural Science Foundation 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.2c02303
Reference62 articles.
1. Atroposelective Synthesis of Axially Chiral Biaryl Compounds
2. A twist of nature – the significance of atropisomers in biological systems
3. Recent Advances in Catalytic Asymmetric Construction of Atropisomers
4. Recent advances in the synthesis of axially chiral biarylsviatransition metal-catalysed asymmetric C–H functionalization
5. Stereoselective construction of atropisomers featuring a C–N chiral axis
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4. Chiral Transient Ligand Enabled Enantioselective Synthesis of Atropisomers Decorated with Unactivated Olefins via a Palladium-Catalyzed C–H Olefination;Organic Letters;2023-10-16
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