C-H functionalization of imidazo[1,5-a]pyridines: a metal-free approach for methylene insertion to access C(sp2)-C(sp3)-H-C(sp2) bond formation
Title | C-H functionalization of imidazo[1,5-a]pyridines: a metal-free approach for methylene insertion to access C(sp2)-C(sp3)-H-C(sp2) bond formation |
Publication Type | Journal Article |
Year of Publication | 2024 |
Authors | Mahajan, S, Sawant, SD |
Journal | ACS Omega |
Volume | 9 |
Issue | 50 |
Pagination | 49071-49080 |
Date Published | DEC |
Type of Article | Article |
ISSN | 2470-1343 |
Abstract | Formaldehyde has been used as a solvent and a source of carbon to insert a methylene group for bridging two imidazo[1,5-a]pyridine molecules without using any metal catalysis. This strategy has been extended on other alkyl-, aryl-, and heteroaryl aldehydes as well. This C(sp2)-C(sp3)-H-C(sp2) bond forming reaction proceeds via C(sp2)H functionalization of imidazo[1,5-a]pyridine and was applied on a wide range of substrates offering moderate to good yields of methylene-bridged/inserted bis-imidazo[1,5-a]pyridines. Most importantly, as an application, the bis-heteroarene product has been demonstrated as a ligand. The ligand-like behavior of bis-imidazo[1,5-a]pyridines has been demonstrated as an extension of current methodology. This reaction works well at the gram scale level. |
DOI | 10.1021/acsomega.4c03823 |
Type of Journal (Indian or Foreign) | Foreign |
Impact Factor (IF) | 4.1 |
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