A four-component coupling process involving sequential reactions of aldehydes, primary amines, acid chlorides, and nucleophiles has been developed to prepare multifunctional substrates that may be employed in subsequent ring-forming reactions to generate a diverse array of functionalized heterocyclic scaffolds. This new approach to diversity-oriented synthesis was then applied to the first total synthesis of the isopavine alkaloid (±)-roelactamine. © 2007 American Chemical Society.
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Sunderhaus, J. D., Dockendorff, C., & Martin, S. F. (2007). Applications of multicomponent reactions for the synthesis of diverse heterocyclic scaffolds. Organic Letters, 9(21), 4223–4226. https://doi.org/10.1021/ol7018357