SET-oxidative photocyclization reactions of N -(α-trimethylsilyl)- N -phenylglycinates with N -substituted maleimides: a role of silyl group in photocyclization
Abstract
-phenylglycinates with maleimides led to the formation of tetrahydroquinoline derivatives efficiently. These observations reveal that the silyl group adjacent to the nitrogen atom plays a crucial role in enabling a successful SET-oxidative cyclization reaction. Overall, this reaction protocol can expand the range of amine substrates in the diverse SET-oxidative photochemical reactions.
Fields of Study & Subjects
Radical Photochemical Reactions
Chemical Reactions and Mechanisms
Photopolymerization techniques and applications
Publication details
- Journal / source
- Organic & Biomolecular Chemistry
- Volume
- 24
- Issue
- 10
- Pages
- 2102–2110
- Publication date
- 1 January 2026
- Language
- EN