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Readily Accessible and Highly Efficient Ferrocene‐Based Amino‐Phosphine‐Alcohol (f‐Amphol) Ligands for Iridium‐Catalyzed Asymmetric Hydrogenation of Simple Ketones
Ist Teil von
Chemistry : a European journal, 2017-01, Vol.23 (4), p.970-975
Ort / Verlag
Germany: Wiley Subscription Services, Inc
Erscheinungsjahr
2017
Quelle
Wiley Online Library - AutoHoldings Journals
Beschreibungen/Notizen
We have successfully developed a series of novel and modular ferrorence‐based amino‐phosphine‐alcohol (f‐Amphol) ligands, and applied them to iridium‐catalyzed asymmetric hydrogenation of various simple ketones to afford the corresponding chiral alcohols with excellent enantioselectivities and conversions (98–99.9 % ee, >99 % conversion, turnover number up to 200 000). Control experiments and density functional theory (DFT) calculations have shown that the hydroxyl group of our f‐Amphol ligands played a key role in this asymmetric hydrogenation.
Pure and simple: A series of novel and modular ferrorence‐based amino‐phosphine‐alcohol (f‐Amphol) ligands have been developed and applied to iridium‐catalyzed asymmetric hydrogenation of various simple ketones to afford the corresponding chiral alcohols with excellent enantioselectivities and conversions (see scheme). Control experiments and density functional calculations have shown that the hydroxyl group of the f‐Amphol ligands played a key role in this asymmetric hydrogenation.