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- W2008009879 abstract "Abstract Practical conditions for the synthesis of 4‐substituted N ‐protected piperidines through CuCN·2LiBr‐catalyzed organozinc additions to 1‐acylpyridinium salts and subsequent hydrogen‐transfer hydrogenation have been established. The reaction sequence is performed at room temperature and provides 4‐substituted N ‐protected piperidines in excellent overall yields without the isolation of intermediate dihydropyridines. In those cases in which the organozinc addition results in mixtures of 2‐ and 4‐substituted dihydropyridines, the 2‐substituted isomers are efficiently scavenged with maleic anhydride and subsequently removed by a mild extractive workup with NaHCO 3 (sat.). The N ‐acyl group can conveniently be exchanged from N ‐phenoxycarbonyl to N ‐ t Boc, thus allowing orthogonal deprotection strategies. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003)" @default.
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- W2008009879 date "2003-11-19" @default.
- W2008009879 modified "2023-09-23" @default.
- W2008009879 title "Efficient Solution-Phase Parallel Synthesis of 4-SubstitutedN-Protected Piperidines" @default.
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- W2008009879 doi "https://doi.org/10.1002/ejoc.200300387" @default.
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