Borohydride intermediates pave the way for magnesium-catalysed enantioselective ketone reduction
A magnesium precatalyst for the highly enantioselective hydro-boration of CO bonds is reported. The mechanistic basis of the unprecedented selectivity of this transformation has been investi-gated experimentally by isolation of catalytic intermediates and theoretically by DFT calculations. The facil...
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| Main Authors: | , , , |
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| Format: | Article (Journal) |
| Language: | English |
| Published: |
2020
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| In: |
Chemical communications
Year: 2019, Volume: 56, Issue: 8, Pages: 1203-1206 |
| ISSN: | 1364-548X |
| DOI: | 10.1039/C9CC09111D |
| Online Access: | Verlag, Volltext: https://doi.org/10.1039/C9CC09111D Verlag: https://pubs.rsc.org/en/content/articlelanding/2020/cc/c9cc09111d |
| Author Notes: | Vladislav Vasilenko, Clemens K. Blasius, Hubert Wadepohl and Lutz H. Gade |
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| 520 | |a A magnesium precatalyst for the highly enantioselective hydro-boration of CO bonds is reported. The mechanistic basis of the unprecedented selectivity of this transformation has been investi-gated experimentally by isolation of catalytic intermediates and theoretically by DFT calculations. The facile formation of a magnesium borohydride species is critical in overcoming competing pathways in the selectivity-determining insertion step. | ||
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