Asymmetric Photoredox Catalytic Minisci-Type Reactions of α-Bromide Amides
An asymmetric photoredox catalytic Minisci-type reaction between α-bromide amides and imine-containing azaarenes has been successfully developed. This catalyst system employs a chiral phosphoric acid alongside 3DPAFIPN as a photosensitizer. The reaction produces a diverse array of valuable amides, featuring azaarene-substituted tertiary carbon stereocenters at the β-position, in high yields (up to 85%) and good to excellent enantioselectivities (up to >99% enantiomeric excess (ee)). Importantly, this work marks the first example of asymmetric radical addition to simple azaarenes utilizing radicals functionalized with electron-withdrawing carbonyl groups, which are conventionally considered unfavorable for such transformations, especially in an enantioselective manner.
Authors
- Zhiyong Jiang (ORCID: https://orcid.org/0000-0002-6350-7429)
- Yanli Yin (ORCID: https://orcid.org/0000-0002-0013-3116)
- Qifu Li (ORCID: https://orcid.org/0000-0003-3904-410X)
- Tianju Shao (ORCID: https://orcid.org/0009-0000-2167-9882)
- Xiaowei Zhao (ORCID: https://orcid.org/0000-0002-2313-8083)
Institutions
- Henan University (CN)
- Henan Normal University (CN)
Publication Details
- Journal
- Organic Letters
- Published
- 2025-01-23
- DOI
- https://doi.org/10.1021/acs.orglett.4c04791
- Citations
- 2
- Primary Topic
- Radical Photochemical Reactions
- Type
- article
- Field-Weighted Citation Impact
- 1.87
Funders
- National Natural Science Foundation of China