Add to ORKGAbstract―Synthesis of amine libraries from aldehydes via the liquid-phase parallel reductive amination with a simple scavenger (a Dowex resin) is described. Three parallel protocols are compared: reactions in well plates, SynCore apparatus, glass vials (without specific equipment). The presented detailed protocols can be useful for practical training of students
The imines were generated in situ from carbonyl compounds and amines, which undergo smooth reduction...
A simple, solventless procedure for reductive amination that results in an impressive color change. ...
Zinc powder in aqueous alkaline media was employed to perform reductive amination of aldehydes with ...
Preparation of a small library of secondary amino acids was achieved by solution-phase organic synth...
A poster containing visuals and text describing an undergraduate research project completed at the U...
A parallel reductive amination of heteroaromatic amines has been performed using a combination of Zn...
Abstract―Key aspects of differences between liquid-phase parallel synthesis and preparation of a sin...
A comparative study of various widely used methods of reductive amination is reported. Specifically,...
We report a catalytic reductive alkylation reaction of primary or secondary amines with carboxylic a...
1252-1259Reductive amination of aldehydes to produce secondary amines at room-temperature by in sit...
Combinatorial chemistry is a means of rapidly generating large numbers of diverse molecules for the ...
Homoallylic amines prepared via addition of allylsilanes often require preformed imine substrates, m...
Novel aldehyde-functionalized ionic liquids have been synthesized and used as scavengers for primary...
A range of alternative, more environmentally conservative solvents have been evaluated for use withi...
We disclose in this study a Ni6AlOx catalyst prepared by coprecipitation for the reductive amination...
The imines were generated in situ from carbonyl compounds and amines, which undergo smooth reduction...
A simple, solventless procedure for reductive amination that results in an impressive color change. ...
Zinc powder in aqueous alkaline media was employed to perform reductive amination of aldehydes with ...
Preparation of a small library of secondary amino acids was achieved by solution-phase organic synth...
A poster containing visuals and text describing an undergraduate research project completed at the U...
A parallel reductive amination of heteroaromatic amines has been performed using a combination of Zn...
Abstract―Key aspects of differences between liquid-phase parallel synthesis and preparation of a sin...
A comparative study of various widely used methods of reductive amination is reported. Specifically,...
We report a catalytic reductive alkylation reaction of primary or secondary amines with carboxylic a...
1252-1259Reductive amination of aldehydes to produce secondary amines at room-temperature by in sit...
Combinatorial chemistry is a means of rapidly generating large numbers of diverse molecules for the ...
Homoallylic amines prepared via addition of allylsilanes often require preformed imine substrates, m...
Novel aldehyde-functionalized ionic liquids have been synthesized and used as scavengers for primary...
A range of alternative, more environmentally conservative solvents have been evaluated for use withi...
We disclose in this study a Ni6AlOx catalyst prepared by coprecipitation for the reductive amination...
The imines were generated in situ from carbonyl compounds and amines, which undergo smooth reduction...
A simple, solventless procedure for reductive amination that results in an impressive color change. ...
Zinc powder in aqueous alkaline media was employed to perform reductive amination of aldehydes with ...