Recent advances in transition metal-free annulation toward heterocycle diversity based on the C-N bond cleavage of enaminone platform

Enaminones and analogous stable enamines are well known as platform building blocks in organic synthesis for the construction of heterocyclic compounds, especially N-heterocycles. To date, enaminones have been successfully employed in the synthesis of various 5- or 6- membered heterocycles. Recently, synthetic protocols accomplished by diversity-oriented annulation reactions based on the C-N bond cleavage of enamines have gained notable success. In this review, the development of the transition metal-free heterocyclic product synthesis based on the annulation reactions of enaminones or analogous enamines featuring a C-N bond cleavage is reviewed.

Automated summary

Enaminones and analogous stable enamines are widely used as platform building blocks in organic synthesis for constructing heterocyclic compounds, especially N-heterocycles. Recently, synthetic protocols based on the C-N bond cleavage of enamines have achieved notable success in the development of transition metal-free heterocyclic product synthesis.