![Selectivities in ionic reductions of alcohols and ketones with triethylsilane/trifluoroacetic acid - ScienceDirect Selectivities in ionic reductions of alcohols and ketones with triethylsilane/trifluoroacetic acid - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0040403996024847-gr1.gif)
Selectivities in ionic reductions of alcohols and ketones with triethylsilane/trifluoroacetic acid - ScienceDirect
![Recent progress towards ionic hydrogenation: Lewis acid catalyzed hydrogenation using organosilanes as donors of hydride ions - RSC Advances (RSC Publishing) DOI:10.1039/C5RA15172D Recent progress towards ionic hydrogenation: Lewis acid catalyzed hydrogenation using organosilanes as donors of hydride ions - RSC Advances (RSC Publishing) DOI:10.1039/C5RA15172D](https://pubs.rsc.org/image/article/2015/RA/c5ra15172d/c5ra15172d-f1_hi-res.gif)
Recent progress towards ionic hydrogenation: Lewis acid catalyzed hydrogenation using organosilanes as donors of hydride ions - RSC Advances (RSC Publishing) DOI:10.1039/C5RA15172D
![Representative reductions with triethylsilane: (a) alcohols; (b) ethers. | Download Scientific Diagram Representative reductions with triethylsilane: (a) alcohols; (b) ethers. | Download Scientific Diagram](https://www.researchgate.net/publication/330642172/figure/fig5/AS:719132353900544@1548465922587/Selectivity-experiments-with-various-functional-groups-a-Reduction-of-acetanilide_Q320.jpg)
Representative reductions with triethylsilane: (a) alcohols; (b) ethers. | Download Scientific Diagram
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