Pyrene-Based Organic Photoredox Catalysts for Carbon–Carbon Bond-Forming Reactions: Reductive Coupling of Aromatic Carbonyl and Imine Compounds
Metal-free photoredox catalysts built upon a pyrene core were developed for carbon-carbon bond-forming reactions. Among these catalysts, a pyrene derivative containing a urea moiety effectively facilitated the reductive coupling of aromatic carbonyl and imine compounds under blue LED irradiation. This process provided the corresponding vicinal diols and diamines in good yields.
Authors
- Shusuke Okamoto (ORCID: https://orcid.org/0000-0002-6102-5848)
- Daisuke Nagai (ORCID: https://orcid.org/0000-0003-4205-822X)
Institutions
- University of Shizuoka (JP)
Publication Details
- Journal
- Organic Letters
- Published
- 2024-09-05
- DOI
- https://doi.org/10.1021/acs.orglett.4c02845
- Citations
- 5
- Primary Topic
- Radical Photochemical Reactions
- Type
- article
- Field-Weighted Citation Impact
- 1.25
Funders
- Japan Society for the Promotion of Science