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- W3197449851 endingPage "5443" @default.
- W3197449851 startingPage "5443" @default.
- W3197449851 abstract "Although there exists a variety of different catalysts for hydroboration of organic substrates such as aldehydes, ketones, imines, nitriles etc., recent evidence suggests that tetra-coordinate borohydride species, formed by activation, redistribution, or decomposition of boron reagents, are the true hydride donors. We then proposed that Me2S-BH3 could also act as a hydride donor for the reduction of various imines, as similar compounds have been observed to reduce carbonyl substrates. This boron reagent was shown to be an effective and chemoselective hydroboration reagent for a wide variety of imines." @default.
- W3197449851 created "2021-09-13" @default.
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- W3197449851 date "2021-09-07" @default.
- W3197449851 modified "2023-09-25" @default.
- W3197449851 title "Imine Reduction with Me2S-BH3" @default.
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- W3197449851 doi "https://doi.org/10.3390/molecules26185443" @default.
- W3197449851 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/8467297" @default.
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- W3197449851 hasPublicationYear "2021" @default.
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