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Enantioselective Construction of Octahydroquinolines via Trienamine-Mediated Diels–Alder Reactions

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journal contribution
posted on 05.04.2019, 12:04 by Taichi Inoshita, Kei Goshi, Yuka Morinaga, Yuhei Umeda, Hayato Ishikawa
A trienamine-mediated asymmetric Diels–Alder reaction using a 5-nitro-2,3-dihydro-4-pyridone derivative as a dienophile in the presence of a secondary amine organocatalyst derived from cis-hydroxyproline was discovered. The reaction provides optically active octahydroquinolines through an endo-selective [4 + 2] cyclization pathway. The following stereoselective denitration, isomerization, and/or hydrogenation generated divergent stereoisomers of decahydroquinolines, which are useful synthons for the total synthesis of Lycopodium alkaloids.

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