Asymmetric Synthesis of Spiropyrazolones by Sequential Organo- and Silver Catalysis

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Abstract

A stereoselective one-pot synthesis of spiropyrazolones through an organocatalytic asymmetric Michael addition and a formal Conia-ene reaction has been developed. Depending on the nitroalkene, the 5-exo-dig-cyclization could be achieved by silver-catalyzed alkyne activation or by oxidation of the intermediate enolate. The mechanistic pathways have been investigated using computational chemistry and mechanistic experiments.

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Hack, D., Dürr, A. B., Deckers, K., Chauhan, P., Seling, N., Rübenach, L., … Enders, D. (2016). Asymmetric Synthesis of Spiropyrazolones by Sequential Organo- and Silver Catalysis. Angewandte Chemie - International Edition, 55(5), 1797–1800. https://doi.org/10.1002/anie.201510602

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