Selective alkylation of amines with alcohols by Cp*-iridium(III) half-sandwich complexes
[Cp*Ir(Pro)Cl] (Pro = prolinato) was identified among a series of Cp*-iridium half-sandwich complexes as a highly reactive and selective catalyst for the alkylation of amines with alcohols. It is active under mild conditions in either toluene or water without the need for base or other additives, to...
Gespeichert in:
| Hauptverfasser: | , , , , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
01/03/2013
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| In: |
Organic letters
Year: 2013, Jahrgang: 15, Heft: 2, Pages: 266-269 |
| ISSN: | 1523-7052 |
| DOI: | 10.1021/ol303075h |
| Online-Zugang: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1021/ol303075h
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| Verfasserangaben: | Alexander Wetzel, Simone Wöckel, Mathias Schelwies, Marion K. Brinks, Frank Rominger, Peter Hofmann, and Michael Limbach |
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| 520 | |a [Cp*Ir(Pro)Cl] (Pro = prolinato) was identified among a series of Cp*-iridium half-sandwich complexes as a highly reactive and selective catalyst for the alkylation of amines with alcohols. It is active under mild conditions in either toluene or water without the need for base or other additives, tolerates a wide range of alcohols and amines, and gives secondary amines in good to excellent isolated yields. | ||
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