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首页> 外文期刊>Applied Organometallic Chemistry >Asymmetric 1,4-conjugation addition of diethylzinc to cyclic enones catalyzed by a self-assembled copper complex
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Asymmetric 1,4-conjugation addition of diethylzinc to cyclic enones catalyzed by a self-assembled copper complex

机译:自组装铜配合物催化二乙基锌向环烯酮的不对称1,4共轭加成

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摘要

A new self-assembled catalyst system based on copper complex was developed for the 1,4-conjugation addition of diethyl zinc to cyclic enones. The self-assembled catalyst was readily prepared from (R)-[1,1 ']binaphthalenyl-2,2'-diamine (1a), (L)-tryptophan (3f) and copper(l) chloride (CuCI). Several enones were found to be suitable substrates in the presence of the self-assembled copper catalyst [10 mol% (R)-1a, 10 mol% (L)-3f and 10 mol% CuCI] under optimized conditions. The desired products were afforded with high isolated yields (up to 98%) and moderate to good enantioselectivities (up to 80% ee) in mild conditions (at 0 °C).
机译:开发了基于铜配合物的新型自组装催化剂体系,用于将二乙基锌与环烯酮进行1,4-共轭加成。自组装催化剂容易由(R)-[1,1']二萘基-2,2'-二胺(1a),(L)-色氨酸(3f)和氯化铜(l)制备。发现在优化条件下,在自组装铜催化剂[10摩尔%(R)-1a,10摩尔%(L)-3f和10摩尔%CuCl]存在下,几种烯酮是合适的底物。在温和的条件下(0°C),所需的产物具有较高的分离收率(高达98%)和中等至良好的对映选择性(高达80%ee)。

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