Abstract
Herein, we first time developed a simple, readily available, clean and efficient CuCN/[bmim][PF6] system for the one-pot synthesis of 3-aminoindolizines using commercially available starting materials which included pyridine-2-carbaldehyde, secondary amines, and terminal alkynes. As well, the CuCN/[bmim][PF6] system was reused six times without any appreciable change in its activity.
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