Nitrogen Heterocycles From Furans: The Aza-Achmatowicz Reaction

All articles of this category The furan nucleus may be considered as a latent 1,4-dicarbonyl group. Expression of this functional equivalence within a generic 2-furylamide results in formation of nitrogen heterocycles in a reaction that may be termed the "Aza-Achmatowicz rearrangement", by analogy with similar transformations of furylcarbinols. Aza-Achmatowicz products may be created in enantioselective form by chemoenzymatic methods, and are useful intermediates in the synthesis of novel carbacephems, unusual aminoacids, azasaccharides, piperidine and izidine alkaloids. This Account reviews the most significant aspects of aza-Achmatowicz chemistry. alkaloids - aminoacids - azasaccharides - carbacephems - enzymes - furans - izidines - piperidines