Acetals as chiral ligands for organomagnesium and organolithium compounds

被引:0
|
作者
Knollmuller, M [1 ]
Gartner, P [1 ]
Letschnig, M [1 ]
机构
[1] Vienna Tech Univ, Inst Organ Chem, A-1060 Vienna, Austria
来源
MONATSHEFTE FUR CHEMIE | 1998年 / 129卷 / 8-9期
关键词
acetals; ligands; chiral; carbonyl addition; stereoselective;
D O I
10.1007/s007060050118
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Five 2-alkoxyoctahydro-7.8,8-trimethyl-4,7-methanobenzofurans were tested as additives for the enantioselective addition of butyllithium and butylmagnesium bromide to benzaldehyde. The selectivity of the reaction was determined by GC. HPLC, and by measurement of the optical rotation of the obtained 1-phenyl-1-pentanol, and the stability of the ligands under the given reaction conditions was investigated. Upon reaction with benzaldehyde, the addition of octahydro-7,8,8-trimethyl-2-(2-(phenylmethoxy)ethoxy)-4,7-methanobenzofuran to butylmagnesium bromide yielded (R)-1-phenyl-1-pentanol with 47% ee.
引用
收藏
页码:953 / 959
页数:7
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