Abstract
An efficient protocol for the intermolecular amidoselenation of alkenes with diphenyl diselenides and acetonitrile has been developed that affords a series of β-amidoselenides in high yields under mild conditions. The preliminary experimental results support the involvement of active benzyl radical species, and a radical pathway was therefore proposed for the reaction.
Keywords: Alkenes, amidoselenation, radical, difunctionalization, β-amido-selenides, transformation.
Graphical Abstract
Call for Papers in Thematic Issues
Catalytic C-H bond activation as a tool for functionalization of heterocycles
The major topic is the functionalization of heterocycles through catalyzed C-H bond activation. The strategies based on C-H activation not only provide straightforward formation of C-C or C-X bonds but, more importantly, allow for the avoidance of pre-functionalization of one or two of the cross-coupling partners. The beneficial impact of ...read more
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