Imines in Stille‐Type Cross‐Coupling Reactions: A Multicomponent Synthesis of α‐Substituted Amides

Abstract

An alternative to nucleophilic chemistry for the construction of α-substituted amides and amine derivatives from imines is provided by the Stille-type coupling of imines with organotin reagents and acid chlorides (see scheme). This Pd-catalyzed reaction is suitable for components with a range of functional groups and has been extended into a four-component-coupling reaction with carbon monoxide. dba=dibenzylideneacetone, RT=room temperature.