化学
铜
结合
硅烷化
特里斯
锂(药物)
路易斯酸
加成反应
催化作用
药物化学
高分子化学
有机化学
医学
数学分析
生物化学
数学
内分泌学
作者
Martin Oestreich,Gertrud Auer,Barbara Weiner
出处
期刊:Synthesis
[Georg Thieme Verlag KG]
日期:2006-07-01
卷期号:2006 (13): 2113-2116
被引量:10
标识
DOI:10.1055/s-2006-942405
摘要
In the course of our investigations directed towards an asymmetric copper-catalyzed silyl transfer from bis(triorganosilyl) zincs onto α,β-unsaturated carbonyl compounds, the presence of Lewis acidic lithium cations and the uncatalyzed background reaction were identified as major causes thwarting appreciable enantioselection. The latter finding underlines once more that copper is often not even required in the conjugate addition of bis(triorganosilyl) zincs and tris(triorganosilyl) zincates alike.
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