Organic Chemistry Frontiers

Abstract 

Metal-free β- and Z-selective hydrocyanation of terminal ynamides using TMSCN and TBAF is described. The transformation proceeds with excellent regio- and stereoselectivity, delivering exclusively Z-configured tertiary enamides. Treatment with TMSOTf promotes clean Z to E isomerization. Simultaneous activation of the nitrile moiety by TMSOTf in the presence of an internal nucleophile induces intramolecular cyclization, yielding piperidine frameworks. The reaction accommodates a range of nucleophiles, enabling the synthesis of structurally diverse and previously inaccessible heterocyclic scaffolds.

 

Reference

β- and Z-selective metal-free cyanation of ynamides: a direct approach to piperidines fused to arenes
Dorian Schutz, Wenwen Yang and Laurence Miesch
Org. Chem. Front.2026 - DOI :10.1039/d6qo00022c

 

Contact

Laurence Miesch, team SOPhy, Institut de Chimie de Strasbourg (UMR 7177).

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