Organocatalysts

DescriptionHighly selective organocatalyst for the Diels-Alder reaction with simple α,β−unsaturated ketones.

Description(2S,3R)-3-(Benzyloxy)-2-((3-(tert-butyl)-2-hydroxybenzyl)amino)-N,N-dimethylbutanamide is an aminophenol organocatalyst developed by the Hoveyda lab for enantioselective addition of allylboron compounds to imines, ketones, and other

Description(2S,3R)-3-(Benzyloxy)-2-((3-(tert-butyl)-2-hydroxybenzyl)amino)-N,N-dimethylbutanamide is an aminophenol organocatalyst developed by the Hoveyda lab for enantioselective addition of allylboron compounds to imines, ketones, and other

Application：Catalyst for:1.Enantioselective organocatalytic transfer hydrogenation of cycloalkenones with tert-Bu Hantzsch ester as source of hydrogen；2.Alkylation of indoles with an α,β-disubstituted α,β-unsaturated aldehyde in the enantioselective

Application：Catalyst for:1.Enantioselective organocatalytic transfer hydrogenation of cycloalkenones with tert-Bu Hantzsch ester as source of hydrogen；2.Alkylation of indoles with an α,β-disubstituted α,β-unsaturated aldehyde in the enantioselective

Application：Catalyst for:1.Enantioselective organocatalytic transfer hydrogenation of cycloalkenones with tert-Bu Hantzsch ester as source of hydrogen；2.Alkylation of indoles with an α,β-disubstituted α,β-unsaturated aldehyde in the enantioselective

(3-Carboxypropyl)trimethylammonium chloride.

(3-Carboxypropyl)trimethylammonium chloride.

(3-Carboxypropyl)trimethylammonium chloride.

(3-Carboxypropyl)trimethylammonium chloride.

(3-Carboxypropyl)trimethylammonium chloride.

(3-Carboxypropyl)trimethylammonium chloride.