The first catalytic asymmetric addition of diethylzinc to aldehyde promoted by chiral thiourea

被引:0
作者
Zhi Guo Qiao
机构
关键词
Chiral thiourea; Diethylzinc; Amino alcohol; C2-symmetric; Enantioselective addition;
D O I
暂无
中图分类号
O621.25 [];
学科分类号
070303 ; 081704 ;
摘要
A series of C2-symmetric and asymmetric chiral thiourea derivatives were synthesized from commercial L-phenylalanine.All of the new compounds have been fully characterized by IR,~1H NMR,13C NMR,MS spectra and elemental analyses.The chiral thioureas were used as chiral ligands in the catalytic enantioselective ethylation of aldehydes with diethylzinc,the corresponding sec-alcohols were gained with excellent enantioselectivities(up to 87.1%ee) and high yields(up to 76.7%) after the conditions were optimized.
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页码:1265 / 1268
页数:4
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  • [1] A Highly Enantioselective Brosted Acid Catalyst for the Strecker Reaction .2 M.Rueping,E.Sugiono,C.Azap. Angew. Chem. Int. Ed . 2006