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Synthesis of 4‑Silapiperidine Building Blocks with N–H Groups Using the Staudinger Reaction

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journal contribution
posted on 09.12.2013, 00:00 by Markus Fischer, Reinhold Tacke
4-Silapiperidines are important skeletons for drug design. In this context, a novel acid-free method for the synthesis of 4-silapiperidine building blocks with N–H groups has been developed, using the Staudinger reaction as the key step. As a proof of principle, the model compounds 13 and 14 were synthesized, starting from Ph2SiCl2 and MeSi­(OMe)3, respectively.

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