The first example of metal-free B(C6F5)3-catalyzed asymmetric reduction amination of ketones with chiral α-methylbenzylamine (α-MBA) using ammonia borane as the reductant is reported. This one-pot method has a broad substrate scope and provides various chiral amines in 81–95% yield with 80–99% de. This protocol was further applied in the total synthesis of cinacalcet
A transition-metal-free direct α-C–H amination of ketones has been developed using commercially avai...
Branching out: An organocatalytic reductive amination of α‐branched ketones using dynamic kinetic re...
A new method for the synthesis of chiral β-aryl amines via chiral phosphoric acid-catalyzed enantios...
A green method for chiral amine synthesis, the direct catalytic asymmetric reductive amination, was ...
The asymmetric direct reductive amination of prochiral ketones with aryl amines using 1-hydrosilatra...
An efficient, general procedure for highly chemoselective reductive mono-alkylation of ammonia with ...
Various 1-acyl-2,4,10-trioxaadamantanes were prepared from the corresponding 1-methoxycarbonyl deriv...
The highly efficient direct catalytic reductive amination of ketones with diphenylmethanamine cataly...
Cyclic amines may be prepared via a sequence of deprotection followed by intramolecular reductive am...
We report the use of benzylamine as the amine component in Hantzsch ester mediated and chiral Brønst...
The first enantioselective organocatalytic reductive amination reaction has been accomplished. The d...
Amines constitute the major targets for the production of a plethora of chemical compounds that have...
The highly efficient, regioselective, and enantioselective transfer hydrogenation of α-keto ketimine...
A one-pot reductive amination of aldehydes and ketones with NaBH4 was developed with a view to provi...
A novel one-pot reductive amination of ketones using the combination Ti(OiPr)4/H2/Pd–C is reported. ...
A transition-metal-free direct α-C–H amination of ketones has been developed using commercially avai...
Branching out: An organocatalytic reductive amination of α‐branched ketones using dynamic kinetic re...
A new method for the synthesis of chiral β-aryl amines via chiral phosphoric acid-catalyzed enantios...
A green method for chiral amine synthesis, the direct catalytic asymmetric reductive amination, was ...
The asymmetric direct reductive amination of prochiral ketones with aryl amines using 1-hydrosilatra...
An efficient, general procedure for highly chemoselective reductive mono-alkylation of ammonia with ...
Various 1-acyl-2,4,10-trioxaadamantanes were prepared from the corresponding 1-methoxycarbonyl deriv...
The highly efficient direct catalytic reductive amination of ketones with diphenylmethanamine cataly...
Cyclic amines may be prepared via a sequence of deprotection followed by intramolecular reductive am...
We report the use of benzylamine as the amine component in Hantzsch ester mediated and chiral Brønst...
The first enantioselective organocatalytic reductive amination reaction has been accomplished. The d...
Amines constitute the major targets for the production of a plethora of chemical compounds that have...
The highly efficient, regioselective, and enantioselective transfer hydrogenation of α-keto ketimine...
A one-pot reductive amination of aldehydes and ketones with NaBH4 was developed with a view to provi...
A novel one-pot reductive amination of ketones using the combination Ti(OiPr)4/H2/Pd–C is reported. ...
A transition-metal-free direct α-C–H amination of ketones has been developed using commercially avai...
Branching out: An organocatalytic reductive amination of α‐branched ketones using dynamic kinetic re...
A new method for the synthesis of chiral β-aryl amines via chiral phosphoric acid-catalyzed enantios...