International audienceSeveral reactive sites of 1,2- and 1,3-ketoamides were successively exploited in two complementary domino transformations for the synthesis of polysubstituted monocyclic or bridged bicyclic cyclohexanes, with the creation of up to six stereogenic centers. In both cases, a chiral bifunctional thiourea organocatalyst allowed efficient control of chirality in the final carbocycle
An upper-rim functionalized calix[4]arenebased thiourea installed onto the (R,R)-1,2-cyclohexanediam...
Nowadays, organocatalysis constitutes the third pillar of asymmetric catalysis, alongside transition...
Michael addition is one of the most important carbon–carbon bond formation reactions. In this study,...
International audienceSeveral reactive sites of 1,2- and 1,3-ketoamides were successively exploited ...
International audiencePolysubstituted chiral cyclohexanes and cyclohexenes are important building bl...
The first organocatalytic asymmetric reaction between 1,4-cyclohexanedione and nitroalkenes have bee...
International audienceA new method has been developed for the enantioselective synthesis of highly f...
Au cours de ces travaux nous nous sommes intéressés au développement de nouvelles transformations én...
High on the list of challenges in organic chemistry is the development of new efficient chiral catal...
International audienceThe first organocatalytic enantio- and diastereoselective conjugate addition o...
In this manuscript, we are particularly interested in the formation of chiral mono- and polycyclic c...
Development of efficient organocatalytic reactions for the facile assembly of synthetically and medi...
In this thesis three efficient and enantioselective organocatalytic domino reactions were developed....
Bifunctional thiourea catalysts have been found to be excellent promoters of the challenging Michael...
The research presented herein explores three aspects of asymmetric catalysis: (1) the development of...
An upper-rim functionalized calix[4]arenebased thiourea installed onto the (R,R)-1,2-cyclohexanediam...
Nowadays, organocatalysis constitutes the third pillar of asymmetric catalysis, alongside transition...
Michael addition is one of the most important carbon–carbon bond formation reactions. In this study,...
International audienceSeveral reactive sites of 1,2- and 1,3-ketoamides were successively exploited ...
International audiencePolysubstituted chiral cyclohexanes and cyclohexenes are important building bl...
The first organocatalytic asymmetric reaction between 1,4-cyclohexanedione and nitroalkenes have bee...
International audienceA new method has been developed for the enantioselective synthesis of highly f...
Au cours de ces travaux nous nous sommes intéressés au développement de nouvelles transformations én...
High on the list of challenges in organic chemistry is the development of new efficient chiral catal...
International audienceThe first organocatalytic enantio- and diastereoselective conjugate addition o...
In this manuscript, we are particularly interested in the formation of chiral mono- and polycyclic c...
Development of efficient organocatalytic reactions for the facile assembly of synthetically and medi...
In this thesis three efficient and enantioselective organocatalytic domino reactions were developed....
Bifunctional thiourea catalysts have been found to be excellent promoters of the challenging Michael...
The research presented herein explores three aspects of asymmetric catalysis: (1) the development of...
An upper-rim functionalized calix[4]arenebased thiourea installed onto the (R,R)-1,2-cyclohexanediam...
Nowadays, organocatalysis constitutes the third pillar of asymmetric catalysis, alongside transition...
Michael addition is one of the most important carbon–carbon bond formation reactions. In this study,...