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trichlorosilane

 
National Institutes of Health

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Highly Cited
2012
Highly Cited
2012
Chiral amines are key components in numerous bioactive molecules. The development of efficient and economical ways to access… Expand
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Highly Cited
2009
Highly Cited
2009
Enantioselective reduction of ketimines 6-10 with trichlorosilane can be catalyzed by the N-methyl valine-derived Lewis-basic… Expand
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Highly Cited
2008
Highly Cited
2008
Lewis bases such as Ph3P=O and HMPA catalyze the 1,4-reduction of alpha,beta-unsaturated ketones with trichlorosilane, and… Expand
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Highly Cited
2007
Highly Cited
2007
Asymmetric reduction of ketimines 1 with trichlorosilane can be catalyzed by N-methylvaline-derived Lewis-basic formamides 3a-d… Expand
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Highly Cited
2006
Highly Cited
2006
[reaction: see text] Aryl ketones were reduced to the corresponding alcohols with excellent enantioselectivity (up to 99.7% ee… Expand
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Highly Cited
2006
Highly Cited
2006
Abstract N -Picolinoyl-(2 S )-(diphenylhydroxymethyl)pyrrolidine was found to work as an organic activator in the reduction of… Expand
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Highly Cited
2006
Highly Cited
2006
Separation rates and resolutions within capillary electrophoretic (CE) systems can be enhanced when surface zeta potentials are… Expand
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Highly Cited
2004
Highly Cited
2004
[reaction: see text] Asymmetric reduction of ketimines 1 with trichlorosilane can be catalyzed by a new N-methyl L-valine derived… Expand
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Highly Cited
2003
Highly Cited
2003
The reduction of tetrachloroaurate or potassium tetrachloropalladate with sodium borohydride in the presence of optically active… Expand
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Highly Cited
1988
Highly Cited
1988
To evaluate the possibilities for preparing monolayer films from trichlorosilane derivatives containing aromatic functional… Expand
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