International audienceThe first example of a catalytic asym. thia hetero-Diels-Alder reaction, in which a chiral Lewis acid activates the thiocarbonyl dienophile, is described. The reactions catalyzed by copper(II)-bis(oxazolines) complexes of three dithioesters with simple dienes (such as cyclopentadiene or 2,3-dimethyl-1,3-butadiene) afford optically active dihydrothiopyrans with ees up to 82%. Some aspects of the reaction were investigated by computational means
A highly efficient enantioselective inverse-electron-demand hetero-Diels–Alder reaction of dioxopyrr...
A chiral bis(oxazoline)-copper complex was immobilized onto mesoporous silica and the resulting hete...
The scope of highly enantioselective and diastereoselective Michael additions of enolsilanes to unsa...
International audienceAsym. thia-Diels-Alder reactions involving new dithio esters bearing a chiral ...
International audienceAsym. thia-Diels-Alder reactions involving new dithio esters bearing a chiral ...
International audienceAsym. thia-Diels-Alder reactions involving new dithio esters bearing a chiral ...
We report a new process to access highly enantioenriched sulfur-based heterocycles by an asymmetric ...
A highly enantioselective hetero-Diels–Alder reaction of Danishefsky’s diene with β,γ-unsaturated α-...
This article summarizes the Lewis acid-catalyzed hetero Diels-Alder reactions of new 1-oxa-1,3-butad...
The highly enantioselective hetero-Diels–Alder reaction of Danishefsky’s diene with glyoxals was dev...
Asymmetric catalysis is one of the most effective ways to control a target molecule’s stereochemistr...
1,3,2-Dithioborolans substituted at the 2-position with various homochiral groups can act as chiral ...
Asymmetric catalysis is one of the most effective ways to control a target molecule’s stereochemistr...
A highly efficient enantioselective inverse-electron-demand hetero-Diels–Alder reaction of dioxopyrr...
1,3,2-Dithioborolans substituted at the 2-position with various homochiral groups can act as chiral ...
A highly efficient enantioselective inverse-electron-demand hetero-Diels–Alder reaction of dioxopyrr...
A chiral bis(oxazoline)-copper complex was immobilized onto mesoporous silica and the resulting hete...
The scope of highly enantioselective and diastereoselective Michael additions of enolsilanes to unsa...
International audienceAsym. thia-Diels-Alder reactions involving new dithio esters bearing a chiral ...
International audienceAsym. thia-Diels-Alder reactions involving new dithio esters bearing a chiral ...
International audienceAsym. thia-Diels-Alder reactions involving new dithio esters bearing a chiral ...
We report a new process to access highly enantioenriched sulfur-based heterocycles by an asymmetric ...
A highly enantioselective hetero-Diels–Alder reaction of Danishefsky’s diene with β,γ-unsaturated α-...
This article summarizes the Lewis acid-catalyzed hetero Diels-Alder reactions of new 1-oxa-1,3-butad...
The highly enantioselective hetero-Diels–Alder reaction of Danishefsky’s diene with glyoxals was dev...
Asymmetric catalysis is one of the most effective ways to control a target molecule’s stereochemistr...
1,3,2-Dithioborolans substituted at the 2-position with various homochiral groups can act as chiral ...
Asymmetric catalysis is one of the most effective ways to control a target molecule’s stereochemistr...
A highly efficient enantioselective inverse-electron-demand hetero-Diels–Alder reaction of dioxopyrr...
1,3,2-Dithioborolans substituted at the 2-position with various homochiral groups can act as chiral ...
A highly efficient enantioselective inverse-electron-demand hetero-Diels–Alder reaction of dioxopyrr...
A chiral bis(oxazoline)-copper complex was immobilized onto mesoporous silica and the resulting hete...
The scope of highly enantioselective and diastereoselective Michael additions of enolsilanes to unsa...