A simple and convenient method was developed for the preparation of hindered tertiary amines via direct reductive amination of ketones with secondary aryl amines, using trichlorosilane as reducing agent and tetramethylethylenediamine (TMEDA) as organic Lewis base activator. A broad range of ketones were reacted with <em>N</em>-methylaniline to afford the corresponding tertiary amine products in high yield. An open transition model was proposed for the reductive step
The reductive amination of ketones and aldehydes with amines has been used as a tool for N-alkylatio...
Nowadays, both secondary and tertiary amines are playing vital roles in modern chemical industry as ...
A novel and efficient method for the preparation of secondary amines by reductive amination of carbo...
A simple and convenient method was developed for the preparation of hindered tertiary amines via dir...
A simple and convenient method was developed for the preparation of hindered tertiary amines via dir...
Abstract: An efficient method for the synthesis of various secondary amines through a titanium(IV)is...
A simple, mild and efficient procedure for obtaining N-methyl secondary amines from aldehydes and ke...
A simple and efficient method for the preparation of secondary N-alkylarylamines via reductive amina...
Abstract: A method for direct reductive amination of aldehydes and ketones, including α,β-unsaturate...
A novel one-pot reductive amination of ketones using the combination Ti(OiPr)4/H2/Pd–C is reported. ...
1252-1259Reductive amination of aldehydes to produce secondary amines at room-temperature by in sit...
A variety of secondary amines were obtained in high isolated yields in the reductive amination of al...
An efficient, general procedure for highly chemoselective reductive mono-alkylation of ammonia with ...
A variety of secondary amines were obtained in high isolated yields in the reductive amination of al...
A green method for chiral amine synthesis, the direct catalytic asymmetric reductive amination, was ...
The reductive amination of ketones and aldehydes with amines has been used as a tool for N-alkylatio...
Nowadays, both secondary and tertiary amines are playing vital roles in modern chemical industry as ...
A novel and efficient method for the preparation of secondary amines by reductive amination of carbo...
A simple and convenient method was developed for the preparation of hindered tertiary amines via dir...
A simple and convenient method was developed for the preparation of hindered tertiary amines via dir...
Abstract: An efficient method for the synthesis of various secondary amines through a titanium(IV)is...
A simple, mild and efficient procedure for obtaining N-methyl secondary amines from aldehydes and ke...
A simple and efficient method for the preparation of secondary N-alkylarylamines via reductive amina...
Abstract: A method for direct reductive amination of aldehydes and ketones, including α,β-unsaturate...
A novel one-pot reductive amination of ketones using the combination Ti(OiPr)4/H2/Pd–C is reported. ...
1252-1259Reductive amination of aldehydes to produce secondary amines at room-temperature by in sit...
A variety of secondary amines were obtained in high isolated yields in the reductive amination of al...
An efficient, general procedure for highly chemoselective reductive mono-alkylation of ammonia with ...
A variety of secondary amines were obtained in high isolated yields in the reductive amination of al...
A green method for chiral amine synthesis, the direct catalytic asymmetric reductive amination, was ...
The reductive amination of ketones and aldehydes with amines has been used as a tool for N-alkylatio...
Nowadays, both secondary and tertiary amines are playing vital roles in modern chemical industry as ...
A novel and efficient method for the preparation of secondary amines by reductive amination of carbo...