Ruthenium catalyzed direct asymmetric reductive amination of simple aliphatic ketones using ammonium iodide and hydrogen
On the direct asymmetric reductive amination of aliphatic ketones to primary amines: By using Ru‐Binaphane as catalyst and NH4I as the amine source, it is possible to aminate prochiral aliphatic ketones with moderate ee values up to 74 %.
Gespeichert in:
| Hauptverfasser: | , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
10 June 2020
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| In: |
European journal of organic chemistry
Year: 2020, Heft: 30, Pages: 4796-4800 |
| ISSN: | 1099-0690 |
| DOI: | 10.1002/ejoc.202000750 |
| Online-Zugang: | Resolving-System, lizenzpflichtig, Volltext: https://doi.org/10.1002/ejoc.202000750 Verlag, lizenzpflichtig, Volltext: https://chemistry-europe.onlinelibrary.wiley.com/doi/full/10.1002/ejoc.202000750 |
| Verfasserangaben: | Tamal Ghosh, Martin Ernst, A. Stephen K. Hashmi, and Thomas Schaub |
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| 520 | |a On the direct asymmetric reductive amination of aliphatic ketones to primary amines: By using Ru‐Binaphane as catalyst and NH4I as the amine source, it is possible to aminate prochiral aliphatic ketones with moderate ee values up to 74 %. | ||
| 650 | 4 | |a Asymmetric reductive amination (ARA) | |
| 650 | 4 | |a Chirality | |
| 650 | 4 | |a Enantioselectivity | |
| 650 | 4 | |a Homogeneous catalysis | |
| 650 | 4 | |a Primary amines | |
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