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Synthesis of 4‑Silapiperidine Building Blocks with N–H Groups Using the Staudinger Reaction
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 sy...
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Published in: | Organometallics 2013-12, Vol.32 (23), p.7181-7185 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | 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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ISSN: | 0276-7333 1520-6041 |
DOI: | 10.1021/om400873w |