Cyanation of glycine derivatives

We report a catalytic oxidative C-H cyanation of glycine derivatives using a simple copper(i) catalyst with NFSI as an oxidant via a radical process to furnish α-cyano glycine derivatives, which are useful intermediates for organic synthesis. CuCl acted as both a one-electron reductant and a transition-metal catalyst in this transformation. NFSI served as a one-electron oxidant and generated a N-centered radical as a H-abstractor. The reaction displayed broad substrate scope and mild reaction conditions.PMID:33623936 | DOI:10.1039/d0cc08126d
Source: Chemical Communications - Category: Chemistry Authors: Source Type: research
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