Abstract
A concise and highly efficient strategy for the synthesis of N-glycosyl imidazole analogues is reported. This reaction is based on a palladium catalysed decarboxylative allylation and three steps, namely, carbamation, decarboxylation and allylation are involved. All the substrates can afford the desired products with excellent yields and selectivities. © Partner Organisations 2014.
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CITATION STYLE
Xiang, S., He, J., Ma, J., & Liu, X. W. (2014). One-pot synthesis of β-N-glycosyl imidazole analogues via a palladium-catalysed decarboxylative allylation. Chemical Communications, 50(32), 4222–4224. https://doi.org/10.1039/c3cc48041k
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