The highly regio- and enantioselective hydroxyamination of aldehydes with <i>in situ</i> generated nitrosocarbonyl compounds from a hydroxamic acid derivative was realized by simple and readily available chiral amine catalysts. The resulting hydroxyamination products were readily converted to the corresponding chiral 1,2-aminoalcohol or allylamine derivatives in one pot
Stereoselective hydroaminations of unactivated alkenes are rare as this represents a very challengin...
An organocatalytic enantioselective Michael addition/aza-cyclization cascade reaction of aldehydes w...
Unusual nonlinear asymmetric amplification and chiral ligand loading effects were discovered for the...
The first example of a highly regio- and enantioselective hydroxyamination of aldehydes with in situ...
Asymmetric alkene hydroamination could be a direct route to valuable chiral amines from abundant fee...
A novel type of chiral oxidants are developed for efficient and enantioselective β-hydroxylation rea...
87 p.The extensive occurrence of nitrogenated compounds in the nature and the promising outlook of s...
The asymmetric formal hydroamination of enamines using a CuH catalyst is reported. The method provid...
We have recently reported a family of hydroxylamine based reagents for the α-oxyacylation, α-oxycarb...
The reaction of aromatic nitroso derivatives with enolizable carbonyl compounds (nitroso aldol react...
Catalysts possessing sufficient activity to achieve intermolecular alkene hydroaminations under mild...
International audienceThe first organocatalytic general, efficient and highly enantioselective α-hyd...
Uthoff F, Sato H, Gröger H. Formal Enantioselective Hydroamination of Non-Activated Alkenes: Transfo...
Typescript (photocopy).The formation of a new carbon-carbon bond is perhaps the most fundamental rea...
Chiral aldehyde catalysis is uniquely suitable for the direct asymmetric α-functionalization of N-un...
Stereoselective hydroaminations of unactivated alkenes are rare as this represents a very challengin...
An organocatalytic enantioselective Michael addition/aza-cyclization cascade reaction of aldehydes w...
Unusual nonlinear asymmetric amplification and chiral ligand loading effects were discovered for the...
The first example of a highly regio- and enantioselective hydroxyamination of aldehydes with in situ...
Asymmetric alkene hydroamination could be a direct route to valuable chiral amines from abundant fee...
A novel type of chiral oxidants are developed for efficient and enantioselective β-hydroxylation rea...
87 p.The extensive occurrence of nitrogenated compounds in the nature and the promising outlook of s...
The asymmetric formal hydroamination of enamines using a CuH catalyst is reported. The method provid...
We have recently reported a family of hydroxylamine based reagents for the α-oxyacylation, α-oxycarb...
The reaction of aromatic nitroso derivatives with enolizable carbonyl compounds (nitroso aldol react...
Catalysts possessing sufficient activity to achieve intermolecular alkene hydroaminations under mild...
International audienceThe first organocatalytic general, efficient and highly enantioselective α-hyd...
Uthoff F, Sato H, Gröger H. Formal Enantioselective Hydroamination of Non-Activated Alkenes: Transfo...
Typescript (photocopy).The formation of a new carbon-carbon bond is perhaps the most fundamental rea...
Chiral aldehyde catalysis is uniquely suitable for the direct asymmetric α-functionalization of N-un...
Stereoselective hydroaminations of unactivated alkenes are rare as this represents a very challengin...
An organocatalytic enantioselective Michael addition/aza-cyclization cascade reaction of aldehydes w...
Unusual nonlinear asymmetric amplification and chiral ligand loading effects were discovered for the...