Large asymmetric amplification originating from solubility differences between the enantiopure and the racemic catalyst is observed in the addition of Grignard reagents to enones. This behaviour is not reaction or catalyst specific and is observed for metal complexes of a variety of chiral diphosphine ligands, extensively used in asymmetric catalysis.</p
The first catalytic enantioselective 1,2-addition of Grignard reagents to ketones is presented. This...
A new protocol for the Cu-catalysed asymmetric conjugate addition of Grignard reagents to coumarins ...
The mechanism of the enantioselective 1,4-addition of Grignard reagents to alpha,beta-unsaturated ca...
Large asymmetric amplification originating from solubility differences between the enantiopure and t...
A series of new copper complexes containing chiral ferrocenyl diphosphine ligands of the Josiphos fa...
It is no longer necessary to use dialkylzinc reagents to obtain enantioselectivities >95% in the ...
A highly regio- and enantioselective copper catalysed direct conjugate addition of Grignard reagents...
Enones in which the carbon-carbon double bond is part of the pharmacologically important 2H -chromen...
Remarkable progress in the enantioselective addition of Grignard reagents to carbonyl compounds has ...
The first catalytic enantioselective 1,2-addition of Grignard reagents to ketones is presented. This...
A new protocol for the Cu-catalysed asymmetric conjugate addition of Grignard reagents to coumarins ...
The mechanism of the enantioselective 1,4-addition of Grignard reagents to alpha,beta-unsaturated ca...
Large asymmetric amplification originating from solubility differences between the enantiopure and t...
A series of new copper complexes containing chiral ferrocenyl diphosphine ligands of the Josiphos fa...
It is no longer necessary to use dialkylzinc reagents to obtain enantioselectivities >95% in the ...
A highly regio- and enantioselective copper catalysed direct conjugate addition of Grignard reagents...
Enones in which the carbon-carbon double bond is part of the pharmacologically important 2H -chromen...
Remarkable progress in the enantioselective addition of Grignard reagents to carbonyl compounds has ...
The first catalytic enantioselective 1,2-addition of Grignard reagents to ketones is presented. This...
A new protocol for the Cu-catalysed asymmetric conjugate addition of Grignard reagents to coumarins ...
The mechanism of the enantioselective 1,4-addition of Grignard reagents to alpha,beta-unsaturated ca...