Phenols can be efficiently reduced by sodium formate and Pd/C as the catalyst in water and in the presence of amines to give the corresponding cyclohexylamines. This reaction works at rt for 12 h or at 60 °C under microwave dielectric heating for 20 min. With the exception of aniline, primary, secondary amines, amino alcohols, and even amino acids can be used as nucleophiles. The reductive process is based on a sustainable hydrogen source and a catalyst that can be efficiently recovered and reused. The protocol was developed into a continuous-flow production of cyclohexylamines in gram scale achieving very efficient preliminary results (TON 32.7 and TOF 5.45 h-1)
The liquid phase hydrogenation of the aromatic cyanohydrin mandelonitrile (C6H5CH(OH)CH2CN) over a c...
Hydrogenation of an imine (N-Cyclohexyl(benzylidene)imine) into a secondary amine (N-Benzylcyclohexy...
HF reaction represents a selective method for the synthesis of aldehydes starting from alkenes. Beca...
Phenols can be efficiently reduced by sodium formate and Pd/C as the catalyst in water and in the pr...
Phenols can be efficiently reduced by sodium formate and Pd/C as the catalyst in water and in the pr...
© 2019 Elsevier Inc. Anilines and cyclohexylamines are currently produced from fossil feedstocks. Ph...
Selective reduction of phenol to cyclohexanone over the Pd/C catalyst in the presence of a hydrogen ...
Phenols, being readily available from naturally abundant lignins, are important future feedstocks fo...
© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Cyclohexylamines are important intermediates in ...
Reductive amination can be carried in i-PrOH/H2O as hydrogen sources using commercially available ir...
Hydrogenation of an imine (N-Cyclohexyl(benzylidene)imine) into a secondary amine (N-Benzylcyclohe...
International audienceA one-pot two-step procedure was developed for the alkylation of amines via re...
We report a procedure for the continuous-flow production of cyclohexanone from phenol on the basis o...
A method of reductive amination without an external hydrogen source is reported. Carbon monoxide is ...
A continuous flow method for the direct conversion of alcohols to amines via a hydrogen borrowing ap...
The liquid phase hydrogenation of the aromatic cyanohydrin mandelonitrile (C6H5CH(OH)CH2CN) over a c...
Hydrogenation of an imine (N-Cyclohexyl(benzylidene)imine) into a secondary amine (N-Benzylcyclohexy...
HF reaction represents a selective method for the synthesis of aldehydes starting from alkenes. Beca...
Phenols can be efficiently reduced by sodium formate and Pd/C as the catalyst in water and in the pr...
Phenols can be efficiently reduced by sodium formate and Pd/C as the catalyst in water and in the pr...
© 2019 Elsevier Inc. Anilines and cyclohexylamines are currently produced from fossil feedstocks. Ph...
Selective reduction of phenol to cyclohexanone over the Pd/C catalyst in the presence of a hydrogen ...
Phenols, being readily available from naturally abundant lignins, are important future feedstocks fo...
© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Cyclohexylamines are important intermediates in ...
Reductive amination can be carried in i-PrOH/H2O as hydrogen sources using commercially available ir...
Hydrogenation of an imine (N-Cyclohexyl(benzylidene)imine) into a secondary amine (N-Benzylcyclohe...
International audienceA one-pot two-step procedure was developed for the alkylation of amines via re...
We report a procedure for the continuous-flow production of cyclohexanone from phenol on the basis o...
A method of reductive amination without an external hydrogen source is reported. Carbon monoxide is ...
A continuous flow method for the direct conversion of alcohols to amines via a hydrogen borrowing ap...
The liquid phase hydrogenation of the aromatic cyanohydrin mandelonitrile (C6H5CH(OH)CH2CN) over a c...
Hydrogenation of an imine (N-Cyclohexyl(benzylidene)imine) into a secondary amine (N-Benzylcyclohexy...
HF reaction represents a selective method for the synthesis of aldehydes starting from alkenes. Beca...