首页> 外文期刊>The Journal of Organic Chemistry >Low-temperature Rh-catalyzed asymmetric 1,4-addition of arylboronic acids to α,β-unsaturated carbonyl compounds
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Low-temperature Rh-catalyzed asymmetric 1,4-addition of arylboronic acids to α,β-unsaturated carbonyl compounds

机译:低温Rh催化芳基硼酸向α,β-不饱和羰基化合物的不对称1,4-加成反应

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摘要

Rhodium-catalyzed asymmetric 1,4-addition of arylboronic acids to α,β-unsaturated carbonyl compounds was achieved at temperatures below 0 C using a Rh/MeO-F_(12)-BIPHEP catalyst. The reaction of cyclohexenone or N-R-maleimide with arylboronic acids proceeded even at -80 C in the presence of the Rh catalyst. In the latter case, high enantioselectivity was observed because a low-temperature method was used, regardless of the type of substituent on maleimide.
机译:使用Rh / MeO-F_(12)-BIPHEP催化剂,在0°C以下的温度下,铑催化了芳基硼酸向α,β-不饱和羰基化合物的不对称1,4-加成反应。环己烯酮或N-R-马来酰亚胺与芳基硼酸的反应甚至在Rh催化剂存在下在-80℃进行。在后一种情况下,观察到高对映选择性,因为使用低温方法,而与马来酰亚胺上取代基的类型无关。

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