Urea Ligand-Promoted Chainwalking Heteroannulation for the Synthesis of 6- and 7-membered Azaheterocycles.

Typical approaches to heterocycle construction require significant changes in synthetic strategy even for a change as minor as increasing the ring size. The ability to access multiple heterocyclic scaffolds through a common synthetic approach, simply through trivial modification of one reaction component, would enable facile access to diverse libraries of structural analogues of core scaffolds. Here, we show that urea-derived ligands effectively promote Pd-mediated chainwalking processes to enable remote heteroannulation for the rapid construction of six- and seven-membered azaheterocycles under essentially identical reaction conditions. This method demonstrates good functional group tolerance and effectively engages sterically hindered substrates. In addition, this reaction is applicable to target-oriented synthesis, demonstrated through the formal synthesis of antimalarial alkaloid galipinine.