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- W2912573902 endingPage "432" @default.
- W2912573902 startingPage "432" @default.
- W2912573902 abstract "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 variety of powerful transformations, even in the presence of water. The focus of this review will be to highlight those catalytic reactions that utilize a silane as a stoichiometric reductant in conjunction with tris(pentafluorophenyl) borane in the reduction of alcohols, carbonyls, or carbonyl-like derivatives." @default.
- W2912573902 created "2019-02-21" @default.
- W2912573902 creator A5026151348 @default.
- W2912573902 creator A5029675366 @default.
- W2912573902 date "2019-01-25" @default.
- W2912573902 modified "2023-10-01" @default.
- W2912573902 title "Tris(pentafluorophenyl)borane-Catalyzed Reactions Using Silanes" @default.
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- W2912573902 doi "https://doi.org/10.3390/molecules24030432" @default.
- W2912573902 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6384582" @default.
- W2912573902 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30691072" @default.
- W2912573902 hasPublicationYear "2019" @default.
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