Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10247096 | Journal of Molecular Catalysis A: Chemical | 2005 | 5 Pages |
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
Jincheng Mao, Boshun Wan, Zhanjin Zhang, Rongliang Wang, Fan Wu, Shiwei Lu,