Journal
LETTERS IN ORGANIC CHEMISTRY
Volume 20, Issue 1, Pages 72-76Publisher
BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/1570178619666220806111324
Keywords
Base-promoted; bromination; C-Br bond forming; imidazo[1,2-alpha]pyridines; hydrocarbons; halide
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A bromination reaction of hydrocarbons with CBr4 as a bromine source, promoted by NaOH, has been developed. The reaction method shows high efficiency and regioselectivity for the synthesis of C3-brominated imidazo[1,2-alpha]pyridines. This method serves as an effective and simple approach for C-X bond construction, providing a supplement to the halide of imidazo[1,2-alpha]pyridines.
A bromination of hydrocarbons with CBr4 as a bromine source, promoted by NaOH, has been developed. The reaction method with high efficiency and regioselectivity for the synthesis of C3-brominated imidazo[1,2-alpha]pyridines. An effective and simple method of C-X bond construction has been developed, which is a supplement to the halide of imidazo[1,2-alpha]pyridines.
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