trichlorosilane

Chiral amines are key components in numerous bioactive molecules. The development of efficient and economical ways to access… Expand

Enantioselective reduction of ketimines 6-10 with trichlorosilane can be catalyzed by the N-methyl valine-derived Lewis-basic… Expand

Lewis bases such as Ph3P=O and HMPA catalyze the 1,4-reduction of alpha,beta-unsaturated ketones with trichlorosilane, and… Expand

Asymmetric reduction of ketimines 1 with trichlorosilane can be catalyzed by N-methylvaline-derived Lewis-basic formamides 3a-d… Expand

[reaction: see text] Aryl ketones were reduced to the corresponding alcohols with excellent enantioselectivity (up to 99.7% ee… Expand

Abstract N -Picolinoyl-(2 S )-(diphenylhydroxymethyl)pyrrolidine was found to work as an organic activator in the reduction of… Expand

Separation rates and resolutions within capillary electrophoretic (CE) systems can be enhanced when surface zeta potentials are… Expand

[reaction: see text] Asymmetric reduction of ketimines 1 with trichlorosilane can be catalyzed by a new N-methyl L-valine derived… Expand

The reduction of tetrachloroaurate or potassium tetrachloropalladate with sodium borohydride in the presence of optically active… Expand

To evaluate the possibilities for preparing monolayer films from trichlorosilane derivatives containing aromatic functional… Expand