SimplePhos ligands proved to be very powerful ligands in the generation of quaternary stereogenic centers by Michael addition of alkenyl-aluminum reagents to cyclic enones. Using commercially available and easily accessible alkenylbromides as alane precursors the present procedure offers a facile access to β-alkenyl-substituted cyclohexanones with high enantioselectivities up to 96%
This mini-review deals with a special, and challenging, aspect of the asymmetric conjugate addition:...
An efficient palladium catalyst is presented for the formation of benzylic quaternary stereocenters ...
Synthetic methods for the selective formation of all carbon quaternary centres in non-cyclic systems...
The main focus of this thesis is the creation of quaternary all-carbon stereogenic centers bearing a...
Trimethyl- and triethylaluminum undergo enantioselective conjugate addition to 3- and 2-substituted ...
Novel aryl and alkenyl aluminum reagents are generated through a halogen/Li exchange-Li/Al transmeta...
Herein a comprehensive study is provided on the asymmetric conjugate addition (ACA) of Grignard reag...
Trimethyl- and triethylaluminum undergo enantioselective conjugate addition to 2- and 3-substituted ...
Catalytic asymmetric syntheses of remote quaternary stereocenters have been developed by copper-cata...
This mini-review deals with a special, and challenging, aspect of the asymmetric conjugate addition:...
International audienceAn NHC–Cu complex catalyzed the asymmetric conjugate addition (ACA) of various...
An NHC–Cu complex catalyzed the asymmetric conjugate addition (ACA) of various Grignard reagents to ...
The asymmetric copper-catalyzed conjugate addition to α-alkylidene cycloalkanones, substituted at th...
The development of catalytic, enantioselective methods for the construction of quaternary stereogeni...
Easily prepared alkenylalanates proved to be excellent nucleophiles for the creation of highly conge...
This mini-review deals with a special, and challenging, aspect of the asymmetric conjugate addition:...
An efficient palladium catalyst is presented for the formation of benzylic quaternary stereocenters ...
Synthetic methods for the selective formation of all carbon quaternary centres in non-cyclic systems...
The main focus of this thesis is the creation of quaternary all-carbon stereogenic centers bearing a...
Trimethyl- and triethylaluminum undergo enantioselective conjugate addition to 3- and 2-substituted ...
Novel aryl and alkenyl aluminum reagents are generated through a halogen/Li exchange-Li/Al transmeta...
Herein a comprehensive study is provided on the asymmetric conjugate addition (ACA) of Grignard reag...
Trimethyl- and triethylaluminum undergo enantioselective conjugate addition to 2- and 3-substituted ...
Catalytic asymmetric syntheses of remote quaternary stereocenters have been developed by copper-cata...
This mini-review deals with a special, and challenging, aspect of the asymmetric conjugate addition:...
International audienceAn NHC–Cu complex catalyzed the asymmetric conjugate addition (ACA) of various...
An NHC–Cu complex catalyzed the asymmetric conjugate addition (ACA) of various Grignard reagents to ...
The asymmetric copper-catalyzed conjugate addition to α-alkylidene cycloalkanones, substituted at th...
The development of catalytic, enantioselective methods for the construction of quaternary stereogeni...
Easily prepared alkenylalanates proved to be excellent nucleophiles for the creation of highly conge...
This mini-review deals with a special, and challenging, aspect of the asymmetric conjugate addition:...
An efficient palladium catalyst is presented for the formation of benzylic quaternary stereocenters ...
Synthetic methods for the selective formation of all carbon quaternary centres in non-cyclic systems...