| 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. 
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											Authors
												Jincheng Mao, Boshun Wan, Zhanjin Zhang, Rongliang Wang, Fan Wu, Shiwei Lu, 
											