Article ID Journal Published Year Pages File Type
4909362 Journal of Saudi Chemical Society 2017 4 Pages PDF
Abstract

An efficient nitrosylation of imidazo[1,2-a]pyridines has been developed using tert-Butyl nitrite (TBN) as the NO resource. The nitrosylation protocol demonstrates broad compatibilities, with various functional groups such as halogen, Me, OMe, COOMe et al. well tolerated. Near quantitative yields could be obtained within the imidazo[1,2-a]pyridine scaffold under the optimized conditions.

Related Topics
Physical Sciences and Engineering Chemical Engineering Chemical Engineering (General)
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