The imines were generated in situ from carbonyl compounds and amines, which undergo smooth reduction with sodium borohydride in an ionic liquid/H<SUB>2</SUB>O solvent system. The reaction conditions were very mild and neutral to afford the corresponding highly functionalized amines in excellent yields
1252-1259Reductive amination of aldehydes to produce secondary amines at room-temperature by in sit...
Formerly, our lab developed a one-pot synthesis for the reductive alkylation of monosubstituted malo...
Abstract: A method for direct reductive amination of aldehydes and ketones, including α,β-unsaturate...
The reductive amination of aromatic aldehydes and aromatic amines, performed in the Brønsted acidic ...
The reductive amination of aromatic aldehydes and aromatic amines, performed in the Brønsted acidic ...
A fast, efficient, and high yielding method for the preparation of amines by reductive amination of ...
1970-1971Reactions of aromatic aldehydes with primary amines give the corresponding secondary amine...
A variety of secondary amines were obtained in high isolated yields in the reductive amination of al...
A variety of secondary amines were obtained in high isolated yields in the reductive amination of al...
AlCl3 has been employed for highly chemoselective reductive amination of carbonyl compounds in etha...
The imines derived in situ from aldehydes and amines undergo smoothly nucleophilic addition with all...
(Chemical Equation Presented) A new strategy has been developed for reductive amination of aldehydes...
A one-pot reductive amination of aldehydes and ketones with NaBH4 was developed with a view to provi...
A one-pot reductive amination of aldehydes and ketones with NaBH4 was developed with a view to provi...
A one-pot reductive amination of aldehydes and ketones with NaBH4 was developed with a view to provi...
1252-1259Reductive amination of aldehydes to produce secondary amines at room-temperature by in sit...
Formerly, our lab developed a one-pot synthesis for the reductive alkylation of monosubstituted malo...
Abstract: A method for direct reductive amination of aldehydes and ketones, including α,β-unsaturate...
The reductive amination of aromatic aldehydes and aromatic amines, performed in the Brønsted acidic ...
The reductive amination of aromatic aldehydes and aromatic amines, performed in the Brønsted acidic ...
A fast, efficient, and high yielding method for the preparation of amines by reductive amination of ...
1970-1971Reactions of aromatic aldehydes with primary amines give the corresponding secondary amine...
A variety of secondary amines were obtained in high isolated yields in the reductive amination of al...
A variety of secondary amines were obtained in high isolated yields in the reductive amination of al...
AlCl3 has been employed for highly chemoselective reductive amination of carbonyl compounds in etha...
The imines derived in situ from aldehydes and amines undergo smoothly nucleophilic addition with all...
(Chemical Equation Presented) A new strategy has been developed for reductive amination of aldehydes...
A one-pot reductive amination of aldehydes and ketones with NaBH4 was developed with a view to provi...
A one-pot reductive amination of aldehydes and ketones with NaBH4 was developed with a view to provi...
A one-pot reductive amination of aldehydes and ketones with NaBH4 was developed with a view to provi...
1252-1259Reductive amination of aldehydes to produce secondary amines at room-temperature by in sit...
Formerly, our lab developed a one-pot synthesis for the reductive alkylation of monosubstituted malo...
Abstract: A method for direct reductive amination of aldehydes and ketones, including α,β-unsaturate...