A practical access to highly enantiomerically pure flavanones by catalytic asymmetric transfer hydrogenation.
about
Biomimetic kinetic resolution: highly enantio- and diastereoselective transfer hydrogenation of aglain ketones to access flavagline natural products.The Development of Phosphine-Free "Tethered" Ruthenium(II) Catalysts for the Asymmetric Reduction of Ketones and Imines.Easy To Synthesize, Robust Organo-osmium Asymmetric Transfer Hydrogenation Catalysts.Convenient and highly efficient routes to 2 H-chromene and 4-chromanone derivatives: iodine-promoted and p-toluenesulfonic acid catalyzed cascade cyclizations of propynols.Utilizing an o-Quinone Methide in Asymmetric Transfer Hydrogenation: Enantioselective Synthesis of Brosimine A, Brosimine B, and Brosimacutin L.A highly enantioselective access to chiral chromanones and thiochromanones via copper-catalyzed asymmetric conjugated reduction of chromones and thiochromones.
P2860
A practical access to highly enantiomerically pure flavanones by catalytic asymmetric transfer hydrogenation.
description
2013 nî lūn-bûn
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2013年の論文
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2013年学术文章
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name
A practical access to highly e ...... metric transfer hydrogenation.
@en
A practical access to highly e ...... metric transfer hydrogenation.
@nl
type
label
A practical access to highly e ...... metric transfer hydrogenation.
@en
A practical access to highly e ...... metric transfer hydrogenation.
@nl
prefLabel
A practical access to highly e ...... metric transfer hydrogenation.
@en
A practical access to highly e ...... metric transfer hydrogenation.
@nl
P2093
P2860
P356
P1476
A practical access to highly e ...... metric transfer hydrogenation.
@en
P2093
Anne Jäger
Laurence Noehringer
Marie-Kristin Lemke
Morris Witt
Olga Kataeva
Peter Metz
Petra Fischer
Pia Schwab
Roland Fröhlich
Sandra Tischer
P2860
P304
11651-11655
P356
10.1002/ANIE.201306500
P407
P577
2013-09-11T00:00:00Z