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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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Language: | English |
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container_end_page | 7185 |
container_issue | 23 |
container_start_page | 7181 |
container_title | Organometallics |
container_volume | 32 |
creator | Fischer, Markus Tacke, Reinhold |
description | 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. |
doi_str_mv | 10.1021/om400873w |
format | article |
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source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
title | Synthesis of 4‑Silapiperidine Building Blocks with N–H Groups Using the Staudinger Reaction |
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