Abstract
Direct C−H bond functionalization through radical pathway has emerged as a powerful and ideal strategy for the synthesis of organic compounds. This review provides an overview of recent developments in radical C−H functionalization of imidazoheterocycles such as imidazo[1,2-a]pyridine, benzo[d]imidazo[2,1-b]thiazole, imidazo[2,1-b]thiazole, imidazo[1,2-a]pyrimidine, imidazo[2,1-a]isoquinoline, imidazo[1,2-a]pyrazine and imidazo[1,2-a]quinoline using organic peroxides, photo/electric-induced protocols, iodine-based reagents, first-row transition metal catalysts (Fe, Mn, Ni and Cu) and inorganic oxidants/or salts. (Figure presented.).
| Original language | English |
|---|---|
| Pages (from-to) | 4226-4255 |
| Number of pages | 30 |
| Journal | Advanced Synthesis and Catalysis |
| Volume | 362 |
| Issue number | 20 |
| DOIs | |
| State | Published - 21 Oct 2020 |
Keywords
- C-heteroatom bond formation
- C−C bond formation
- Heterocycle
- imidazoheterocycle
- radicals; C−H functionalization
- single-electron transfer.
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