摘要:
AbstractA straightforward and unprecedented method towards the synthesis of 3‐silapiperidines is described. The key step involves a formal double nucleophilic substitution reaction between the (bromomethyl)dimethylsilyl chloride and a N,C‐sp2‐1,4‐dianionic species generated from N‐monoprotected allylamines. Subsequent functionalizations are also presented.(© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)