Asymmetric Alkynylation/Lactamization Cascade: An Expeditious Entry to Enantiomerically Enriched Isoindolinones

Abstract An unprecedented Cu I –pybox‐diPh‐catalyzed highly enantioselective (up to >99 % ee ) alkynylation/lactamization cascade has been developed as a general catalytic system for the synthesis of diversely substituted isoindolinones of immense biological importance. The cascade effects one CC and two CN bond‐forming events in one reaction vessel under operationally simple, additive‐free reaction conditions in good to excellent yields. The methodology was further extended to the synthesis of tetrahydroisoquinoline scaffolds common to several biologically active natural products in a two‐step sequence with remarkable selectivity (up to 94 % ee ).