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Tris(pentafluorophenyl)borane-Catalyzed Reactions Using Silanes
The utility of an electron-deficient, air stable, and commercially available Lewis acid tris(pentafluorophenyl)borane has recently been comprehensively explored. While being as reactive as its distant cousin boron trichloride, it has been shown to be much more stable and capable of catalyzing a vari...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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MDPI
2019
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6384582/ https://www.ncbi.nlm.nih.gov/pubmed/30691072 http://dx.doi.org/10.3390/molecules24030432 |