Photoinduced Dearomative Multiple Functionalization of Quinolines to Construct Highly Substituted 3D Frameworks
Abstract Dearomative functionalization of quinolines expands the chemical diversity of highly functionalized 3D frameworks, such as 1,2,3,4- and 5,6,7,8-tetrahydroquinoline derivatives, which are important pharmacophores, with minimal synthetic costs. In this short review, we cover recent reports on the visible-light-induced dearomative functionalization of quinolines with an emphasis on reaction design/strategies and mechanistic studies and provide a theoretical basis for developing further dearomative syntheses in the future. 1 Introduction 2 Dearomative Functionalizations through the Formation of Photoexcited Quinolines 3 Dearomative Functionalizations through the Formation of Photoexcited Reagents/Intermediates 4 Conclusion
Authors
- Yuki Nagashima (ORCID: https://orcid.org/0000-0001-8470-5638)
- Asuha Shimose
Institutions
- Tokyo University of Science (JP)
- Shanghai Institute for Science of Science (CN)
- Japan Science and Technology Agency (JP)
- Institute of Science Tokyo (JP)
- The University of Tokyo (JP)
Publication Details
- Journal
- Synlett
- Published
- 2025-02-18
- DOI
- https://doi.org/10.1055/s-0043-1773519
- Citations
- 2
- Primary Topic
- Radical Photochemical Reactions
- Type
- article
- Field-Weighted Citation Impact
- 1.87
Funders
- Japan Society for the Promotion of Science
- Japan Science and Technology Agency