Enantioselective construction of quaternary N-heterocycles by palladium-catalysed decarboxylative al

Abstract

The enantioselective synthesis of nitrogen-containing heterocycles (N-heterocycles) represents a substantial chemical research effort and resonates across numerous disciplines, including the total synthesis of natural products and medicinal chemistry. In this Article, we describe the highly enantioselective palladium-catalysed decarboxylative allylic alkylation of readily available lactams to form 3,3-disubstituted pyrrolidinones, piperidinones, caprolactams and structurally related lactams. Given the prevalence of quaternary N-heterocycles in biologically active alkaloids and pharmaceutical agents, we envisage that our method will provide a synthetic entry into the de novo asymmetric synthesis of such structures. As an entry for these investigations we demonstrate how the described catalysis affords enantiopure quaternary lactams that intercept synthetic intermediates previously used in the synthesis of the Aspidosperma alkaloids quebrachamine and rhazinilam, but that were previously only available by chiral auxiliary approaches or as racemic mixtures. Nitrogen-containing heterocycles are ubiquitous in natural products, pharmaceuticals and in materials science. Here, the stereoselective synthesis of a wide array of structurally diverse, functionalized lactams by palladium-catalysed enantioselective enolate alkylation is described.

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Behenna, D., Liu, Y., Yurino, T. et al. Enantioselective construction of quaternary N-heterocycles by palladium-catalysed decarboxylative allylic alkylation of lactams. Nature Chem 4, 130–133 (2012). https://doi.org/10.1038/nchem.1222

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