期刊
JOURNAL OF ORGANIC CHEMISTRY
卷 80, 期 3, 页码 1457-1463出版社
AMER CHEMICAL SOC
DOI: 10.1021/jo502386w
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资金
- Research Grants Council of Hong Kong [GRF: PolyU5010/13P]
- State Key Laboratory of Chirosciences
- Croucher Foundation
Direct C-3 arylation of imidazo[1,2-a]pyridines with aryl tosylates and mesylates has been accomplished by employing palladium(II) acetate associated with SPhos (2-dicyclohexylphosphino-2',6'-dimethoxybiphenyl) or L1 (2-(2-(diisopropylphosphino)phenyl)-1-methyl-1H-indole). This catalyst system can be applied to a wide range of aryl sulfonates and shows excellent C-3 regioselectivity of imidazo[1,2-a]pyridine. These results represent the first examples of using tosylate- and mesylate-functionalized arenes as the electrophile partners for this regioselective direct arylation.
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