Site-selective iron-catalyzed C–H alkylation of pyrazinones, azauracils and quinoxalinones
Abstract
Described herein is an unprecedented iron-catalyzed C(sp 2 )–H alkylation of pyrazinone, azauracil, and quinoxalinone analogues using ethers and benzyl derivatives, offering broad scope and high functional group tolerance.
Fields of Study & Subjects
Catalytic C–H Functionalization Methods
Synthesis and Catalytic Reactions
Radical Photochemical Reactions
Publication details
- Journal / source
- Organic Chemistry Frontiers
- Volume
- 13
- Issue
- 9
- Pages
- 2725–2729
- Publication date
- 1 January 2026
- Language
- EN