Article ID Journal Published Year Pages File Type
10247096 Journal of Molecular Catalysis A: Chemical 2005 5 Pages PDF
Abstract
Novel sulfamide-amine alcohols (6) were applied to the catalytic asymmetric addition of diethylzinc to aldehydes, providing (S)-products in high yields and good enantioselectivities. These sulfamide-amie alcohols together with Ti(OiPr)4 were shown to obtain the (R)-products in significant enantiomeric excesses and high yields.
Related Topics
Physical Sciences and Engineering Chemical Engineering Catalysis
Authors
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