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Tetrahedron, ISSN 0040-4020, 2008, Volume 64, Issue 49, pp. 11304 - 11312
l-Pipecolinic acid derived N-formamides have been developed as new Lewis basic organocatalysts that promote the asymmetric reduction of N-aryl ketimines using trichlorosilane as the reducing agent... 
Asymmetric reduction | Acyclic ketimines | l-Pipecolinic acid | Lewis basic organocatalysts | Enantiomers | Schiff bases | Organosilicon compounds
Journal Article
by Wu, PC and Wang, ZY and Cheng, MN and Zhou, L and Sun, J
TETRAHEDRON, ISSN 0040-4020, 12/2008, Volume 64, Issue 49, pp. 11304 - 11312
L-Pipecolinic acid derived N-formamides have been developed as new Lewis basic organocatalysts that promote the asymmetric reduction of N-aryl ketimines using trichlorosilane as the reducing agent... 
CATALYTIC ENANTIOSELECTIVE ADDITION | Acyclic ketimines | ASYMMETRIC TRANSFER HYDROGENATION | AROMATIC KETIMINES | CONVERSION | ALKYLATION | ARYL IMINES | ALLYLATION | CHEMISTRY, ORGANIC | Asymmetric reduction | KETONES | REDUCTION | ESTERS | Lewis basic organocatalysts | L-Pipecolinic acid
Journal Article
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