Enantio- and Diastereoselective Tandem Giese Addition/Homolytic Aromatic Substitution Reaction via Visible-Light Photoredox Catalysis
The wide spectrum of biological activities of tetrahydroquinolines (THQs) has prompted the extensive development of synthetic strategies. While photoredox catalysis has emerged as a powerful approach for THQ synthesis, achieving asymmetry remains challenging due to the high reactivity of the radicals. Here we report enantio- and diastereoselective tandem Giese addition/homolytic aromatic substitution reactions via visible-light photoredox catalysis. Using a chiral oxazaborolidinium ion catalyst and photosensitizer, the reaction of α-aminoalkyl radicals with α,β-unsaturated esters provided high yields (up to 97%) of the desired THQs with high enantio- and diastereoselectivities (up to 99% ee and formation of only trans-diastereomer) in a single step.
Authors
- Jae Yeon Kim (ORCID: https://orcid.org/0000-0002-6131-4914)
- Do Hyun Ryu (ORCID: https://orcid.org/0000-0001-7615-4661)
- Hyemin Jeong (ORCID: https://orcid.org/0009-0004-1604-1816)
- Dong Gyu Kim
- Hwanseok Jung
Institutions
- Dong-A University (KR)
- Sungkyunkwan University (KR)
Publication Details
- Journal
- ACS Catalysis
- Published
- 2025-03-04
- DOI
- https://doi.org/10.1021/acscatal.5c00112
- Citations
- 3
- Primary Topic
- Radical Photochemical Reactions
- Type
- article
- Field-Weighted Citation Impact
- 2.81
Funders
- Korea Basic Science Institute
- National Research Foundation of Korea