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DOI:
10.1055/sos-SD-025-00031
Harcken, C., Science of Synthesis, (2007) 25, 70.
The reduction of acid chlorides with trialkylsilanes has been reported in the literature. The acid chloride is treated with triethylsilane and palladium on carbon as the catalyst at elevated temperature.[40] The method is highly substrate dependent and less suitable for aliphatic acid chlorides than for aromatic ones. The reaction has also been performed with platinum or rhodium complexes as catalysts.[41] The method is used much less frequently than the analogous reduction of thioesters.
References
| [40] | Meeeee, M. M., M. Mee. Meee., (8888) 88, 8888. |
| [41] | Meee, M. M.; Meeeee, M.; Meeeeee, M., M. Meee. Mee. M, (8888), 8888. |
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- 8.Meeeee-Meee, (8888) 88/8, 888.
- 8.Meeeee-Meee, (8888) 8/8e, 888.
- 8.Meeeee-Meee, (8888) M 8, 888.
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