The preparation of a range of asymmetric iron and ruthenium-cyclone complexes, and their application to the asymmetric reduction of a ketone, are described. The enantioselectivity of ketone reduction is influenced by a single chiral centre in the catalyst, as well as by the planar chirality in the catalyst. This represents the first example of asymmetric ketone reduction using an iron cyclone catalyst
On the basis of steric hindrance, one carbonyl group in a diketone can be reduced in a regioselectiv...
The final version of this article is available from Nature Publishing Group at http://dx.doi.org/10....
The final version of this article is available from Nature Publishing Group at http://dx.doi.org/10....
A detailed study has been completed on the asymmetric transfer hydrogenation (ATH) of a series of en...
A detailed study has been completed on the asymmetric transfer hydrogenation (ATH) of a series of en...
A review of recent developments in the use of iron catalysts for asymmetric transformations, includi...
The use of an enantiomerically pure amino alcohol, coupled to a transfer hydrogenation process, in t...
In this review, we consider the main processes for the asymmetric transfer hydrogenation of ketones ...
A series of enantiomerically-pure ruthenium tricarbonyl cyclopentadienone complexes were prepared vi...
A series of enantiomerically-pure ruthenium tricarbonyl cyclopentadienone complexes were prepared vi...
The synthesis of a series of tridentate ligands based on a homochiral 1,2-diamine structure attached...
In this account, we describe the design, synthesis and applications of tethered versions of the Ru(I...
An improved method for the synthesis of tethered ruthenium(II) complexes of monosulfonylated diamine...
A series of kinetic and structural investigations on ruthenium-based catalysts for asymmetric transf...
The nature of ruthenium-amino alcohol precursors in the catalytic cycle of asymmetric hydrogen trans...
On the basis of steric hindrance, one carbonyl group in a diketone can be reduced in a regioselectiv...
The final version of this article is available from Nature Publishing Group at http://dx.doi.org/10....
The final version of this article is available from Nature Publishing Group at http://dx.doi.org/10....
A detailed study has been completed on the asymmetric transfer hydrogenation (ATH) of a series of en...
A detailed study has been completed on the asymmetric transfer hydrogenation (ATH) of a series of en...
A review of recent developments in the use of iron catalysts for asymmetric transformations, includi...
The use of an enantiomerically pure amino alcohol, coupled to a transfer hydrogenation process, in t...
In this review, we consider the main processes for the asymmetric transfer hydrogenation of ketones ...
A series of enantiomerically-pure ruthenium tricarbonyl cyclopentadienone complexes were prepared vi...
A series of enantiomerically-pure ruthenium tricarbonyl cyclopentadienone complexes were prepared vi...
The synthesis of a series of tridentate ligands based on a homochiral 1,2-diamine structure attached...
In this account, we describe the design, synthesis and applications of tethered versions of the Ru(I...
An improved method for the synthesis of tethered ruthenium(II) complexes of monosulfonylated diamine...
A series of kinetic and structural investigations on ruthenium-based catalysts for asymmetric transf...
The nature of ruthenium-amino alcohol precursors in the catalytic cycle of asymmetric hydrogen trans...
On the basis of steric hindrance, one carbonyl group in a diketone can be reduced in a regioselectiv...
The final version of this article is available from Nature Publishing Group at http://dx.doi.org/10....
The final version of this article is available from Nature Publishing Group at http://dx.doi.org/10....