Asymmetric addition of diethylzinc to ketones promoted by tartaric acid derivatives
A Hui, J Zhang, Z Wang
Index: Hui, Ailing; Zhang, Jintang; Wang, Zhiyong Synthetic Communications, 2008 , vol. 38, # 14 p. 2374 - 2384
Full Text: HTML
Citation Number: 9
Abstract
Abstract The preparation of new sulfonamide ligands derived from L-tartaric acid and camphor sulfonyl chloride are described. The employment in the titanium tetraisopropoxide- promoted enantioselective addition of diethylzinc to ketones has been studied. The best enantiomeric excess is up to 99% with 7 mol% catalyst loading at room temperature.
Related Articles:
[Bioorganic and Medicinal Chemistry, , vol. 21, # 7 p. 1911 - 1917]