Design of Photoredox-Catalyzed Giese-Type Reaction for the Synthesis of Chiral Quaternary α-Aryl Amino Acid Derivatives via Clayden Rearrangement
Author:
Affiliation:
1. Departments of Pharmacology and Toxicology and Chemistry and Biochemistry, University of Arizona, Tucson, Arizona 85721-0207, United States
Funder
National Institute of General Medical Sciences
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.2c02029
Reference59 articles.
1. Recent progress on the stereoselective synthesis of acyclic quaternary α-amino acids
2. Conformationally Constrained Analogues ofL-Glutamate as Subtype-Selective Modulators of Metabotropic Glutamate Receptors
3. Aldose reductase inhibitor increases doxorubicin-sensitivity of colon cancer cells and decreases cardiotoxicity
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