We describe the direct construction of all-carbon quaternary stereocenters via α-photoalkylation of β-ketocarbonyls with high efficacy and enantioselectivities by merging photoredox catalysis and primary amine catalysis. The open-shell photoradical approach enables asymmetric α-alkylations that are difficult under thermal conditions
There is a growing need in organic synthesis for efficient methodologies for the asymmetric synthesi...
International audienceThe symmetry breaking of meso primary diols bearing a tetrahydropyran ring was...
An expedited method has been developed for the enantioselective synthesis of highly functionalized d...
An important goal of modern organic chemistry is to develop new catalytic strategies for enantiosele...
Herein, a visible-light mediated strategy unlocking a family of cyclic β-amino carbonyl derivatives ...
This study reports the catalytic deracemization of ketones bearing stereocenters in the alpha-positi...
Herein, a visible-light mediated strategy unlocking a family of cyclic β-amino carbonyl derivatives ...
The direct, asymmetric α-amination of aldehydes has been accomplished via a combination of photoredo...
An important goal of modern organic chemistry is to develop new catalytic strategies for enantiosele...
We describe the asymmetric addition of unactivated α-branched cyclic ketones to allenamides catalyze...
The synthesis of stereochemically complex molecules in the pharmaceutical and agrochemical industrie...
Zusammenfassung Quaternary stereocenters are found in numerous bioactive molecules. The Tsuji-Trost ...
International audienceThe symmetry breaking of meso primary diols bearing a tetrahydropyran ring was...
International audienceThe symmetry breaking of meso primary diols bearing a tetrahydropyran ring was...
International audienceThe symmetry breaking of meso primary diols bearing a tetrahydropyran ring was...
There is a growing need in organic synthesis for efficient methodologies for the asymmetric synthesi...
International audienceThe symmetry breaking of meso primary diols bearing a tetrahydropyran ring was...
An expedited method has been developed for the enantioselective synthesis of highly functionalized d...
An important goal of modern organic chemistry is to develop new catalytic strategies for enantiosele...
Herein, a visible-light mediated strategy unlocking a family of cyclic β-amino carbonyl derivatives ...
This study reports the catalytic deracemization of ketones bearing stereocenters in the alpha-positi...
Herein, a visible-light mediated strategy unlocking a family of cyclic β-amino carbonyl derivatives ...
The direct, asymmetric α-amination of aldehydes has been accomplished via a combination of photoredo...
An important goal of modern organic chemistry is to develop new catalytic strategies for enantiosele...
We describe the asymmetric addition of unactivated α-branched cyclic ketones to allenamides catalyze...
The synthesis of stereochemically complex molecules in the pharmaceutical and agrochemical industrie...
Zusammenfassung Quaternary stereocenters are found in numerous bioactive molecules. The Tsuji-Trost ...
International audienceThe symmetry breaking of meso primary diols bearing a tetrahydropyran ring was...
International audienceThe symmetry breaking of meso primary diols bearing a tetrahydropyran ring was...
International audienceThe symmetry breaking of meso primary diols bearing a tetrahydropyran ring was...
There is a growing need in organic synthesis for efficient methodologies for the asymmetric synthesi...
International audienceThe symmetry breaking of meso primary diols bearing a tetrahydropyran ring was...
An expedited method has been developed for the enantioselective synthesis of highly functionalized d...