A highly enantioselective method for the copper-catalyzed desymmetrization of oxabenzonorbornadienes with aluminum reagents and SimplePhos as chiral ligand has been developed. The same reaction with Grignard reagents is also reported. A wide range of alkyl chains have been used with moderate to high enantioselectivity and high trans selectivity. The transfer of a methyl group is also reported with high enantiomeric and diastereomeric excess and yields for different substrates. We finally have been able to perform the first trans enantioselective desymmetrization of oxabenzonorbornadienes with an aromatic group
The highly regio- and enantioselective (up to >99:1 dr, up to 99:1 er) desymmetrization of meso-1,4-...
The synthesis of heterocycles using transition metal catalysis is a topic of broad interest in the f...
The diastereo- and enantioselective reductive coupling of vinylazaarenes with N-Boc aldimines is des...
The desymmetrization of oxabenzonorbornadienes with aluminum reagents and SimplePhos as chiral ligan...
A highly efficient method is reported for the asymmetric ring opening of oxabicyclic alkenes with or...
In this Account, recent advances in catalytic asymmetric conjugate addition of Grignard reagents are...
In this Account, recent advances in catalytic asymmetric conjugate addition of Grignard reagents are...
Enantioselective copper catalyzed allylic alkylation is a powerful carbon-carbon bond forming reacti...
Catalytic asymmetric conjugate addition reactions represent a powerful strategy to access chiral mol...
An unprecedented copper phosphoramidite catalyzed enantioselective alkylative ring-opening reaction ...
An unprecedented copper phosphoramidite catalyzed enantioselective alkylative ring-opening reaction ...
The reaction of allylic compounds with alkyl Grignard reagents in the presence of a catalytic amount...
The research carried out in this thesis was directed towards the development of new, catalytic asymm...
Natural chiral compounds, like sugars and aminoacids, are biologically synthesized as a single enant...
This thesis describes the study of organozirconium reagents used in copper-catalyzed asymmetric synt...
The highly regio- and enantioselective (up to >99:1 dr, up to 99:1 er) desymmetrization of meso-1,4-...
The synthesis of heterocycles using transition metal catalysis is a topic of broad interest in the f...
The diastereo- and enantioselective reductive coupling of vinylazaarenes with N-Boc aldimines is des...
The desymmetrization of oxabenzonorbornadienes with aluminum reagents and SimplePhos as chiral ligan...
A highly efficient method is reported for the asymmetric ring opening of oxabicyclic alkenes with or...
In this Account, recent advances in catalytic asymmetric conjugate addition of Grignard reagents are...
In this Account, recent advances in catalytic asymmetric conjugate addition of Grignard reagents are...
Enantioselective copper catalyzed allylic alkylation is a powerful carbon-carbon bond forming reacti...
Catalytic asymmetric conjugate addition reactions represent a powerful strategy to access chiral mol...
An unprecedented copper phosphoramidite catalyzed enantioselective alkylative ring-opening reaction ...
An unprecedented copper phosphoramidite catalyzed enantioselective alkylative ring-opening reaction ...
The reaction of allylic compounds with alkyl Grignard reagents in the presence of a catalytic amount...
The research carried out in this thesis was directed towards the development of new, catalytic asymm...
Natural chiral compounds, like sugars and aminoacids, are biologically synthesized as a single enant...
This thesis describes the study of organozirconium reagents used in copper-catalyzed asymmetric synt...
The highly regio- and enantioselective (up to >99:1 dr, up to 99:1 er) desymmetrization of meso-1,4-...
The synthesis of heterocycles using transition metal catalysis is a topic of broad interest in the f...
The diastereo- and enantioselective reductive coupling of vinylazaarenes with N-Boc aldimines is des...