BINOL derived monodentate acylphosphite ligands for homogeneously catalyzed enantioselective hydrogenation

被引：26
|
作者：
Korostylev, A
Monsees, A
Fischer, C
Borner, A
机构：
[1] Univ Rostock, Leibniz Inst Organ Katal, D-18055 Rostock, Germany
[2] Degussa AG, Projekthuas Katal, Geschaftsbereich Creavis, Ind Hoechst, D-65926 Frankfurt, Germany
[3] Univ Rostock, Fachbereich Chem, D-18059 Rostock, Germany
来源：
TETRAHEDRON-ASYMMETRY | 2004年 / 15卷 / 06期
关键词：
D O I：
10.1016/j.tetasy.2004.01.012
中图分类号：
O61 [无机化学];
学科分类号：
070301 ; 081704 ;
摘要：
Enantiopure acylphosphites have been prepared based upon chiral nonsubstituted and 3,3'-disubstituted binaphthols in order to elucidate steric and electronic effects on the Rh(I)-catalyzed asymmetric hydrogenation of functionalized olefins. With these new types of ligands, up to 80% ee was obtained. Rate as well as enantio selectivity of the hydrogenation were strongly dependent on the precatalyst preparation and substitution pattern of the ligand. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码：1001 / 1005
页数：5
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