A comparative study of various widely used methods of reductive amination is reported. Specifically, such reducing agents as H 2, Pd/C, hydride reagents [NaBH 4, NaBH 3 CN, NaBH(OAc) 3 ], and CO/Rh 2 (OAc) 4 system were considered. For understanding the selectivity and activity of the reducing agents reviewed herein, different classes of starting materials were tested, including aliphatic and aromatic amines, as well as aliphatic and aromatic aldehydes and ketones. Most important advantages and drawbacks of the methods, such as selectivity of the target amine formation and toxicity of the reducing agents were compared. Methods were also considered from the viewpoint of green chemistry. © Georg Thieme Verlag Stuttgart · New York-Synthesis
We developed solvent-free reductive amination without an external hydrogen source using iron pentaca...
1970-1971Reactions of aromatic aldehydes with primary amines give the corresponding secondary amine...
The superior reduction reaction of amineoffered 68% yield and time stability of successful product b...
Abstract: A method for direct reductive amination of aldehydes and ketones, including α,β-unsaturate...
A range of alternative, more environmentally conservative solvents have been evaluated for use withi...
A range of alternative, more environmentally conservative solvents have been evaluated for use withi...
Reductive amination plays a paramount role in pharmaceutical and medicinal chemistry owing to its sy...
Preparation of a small library of secondary amino acids was achieved by solution-phase organic synth...
We report a catalytic reductive alkylation reaction of primary or secondary amines with carboxylic a...
We report a catalytic reductive alkylation reaction of primary or secondary amines with carboxylic a...
A parallel reductive amination of heteroaromatic amines has been performed using a combination of Zn...
Alkyl formates in the presence of basic additives can serve as a reagent in the direct reductive ami...
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...
We developed solvent-free reductive amination without an external hydrogen source using iron pentaca...
We developed solvent-free reductive amination without an external hydrogen source using iron pentaca...
1970-1971Reactions of aromatic aldehydes with primary amines give the corresponding secondary amine...
The superior reduction reaction of amineoffered 68% yield and time stability of successful product b...
Abstract: A method for direct reductive amination of aldehydes and ketones, including α,β-unsaturate...
A range of alternative, more environmentally conservative solvents have been evaluated for use withi...
A range of alternative, more environmentally conservative solvents have been evaluated for use withi...
Reductive amination plays a paramount role in pharmaceutical and medicinal chemistry owing to its sy...
Preparation of a small library of secondary amino acids was achieved by solution-phase organic synth...
We report a catalytic reductive alkylation reaction of primary or secondary amines with carboxylic a...
We report a catalytic reductive alkylation reaction of primary or secondary amines with carboxylic a...
A parallel reductive amination of heteroaromatic amines has been performed using a combination of Zn...
Alkyl formates in the presence of basic additives can serve as a reagent in the direct reductive ami...
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...
We developed solvent-free reductive amination without an external hydrogen source using iron pentaca...
We developed solvent-free reductive amination without an external hydrogen source using iron pentaca...
1970-1971Reactions of aromatic aldehydes with primary amines give the corresponding secondary amine...
The superior reduction reaction of amineoffered 68% yield and time stability of successful product b...