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首页> 外文期刊>Organic letters >Direct catalytic asymmetric Mannich-type reactions of gamma-butenolides: Effectivenes of Bronsted acid in chiral metal catalysis
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Direct catalytic asymmetric Mannich-type reactions of gamma-butenolides: Effectivenes of Bronsted acid in chiral metal catalysis

机译:γ-丁烯内酯的直接催化不对称曼尼希型反应:布朗斯台德酸在手性金属催化中的有效性

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摘要

Direct catalytic asymmetric Mannich-type reactions of gamma-butenolides are described. A chiral Lewis acid/amine base/Bronsted acid combination was used to catalyze a gamma-addition of gamma-butenolides to N-diphenylphosphinoyl imines, affording the products in up to >99% yield, anti/syn = >97:3, and 84% ee. The use of a catalytic amount of TfOH in addition to La(OTf)(3)/Me-PyBox/TMEDA was important for improving yield and stereoselectivity.
机译:描述了γ-丁烯内酯的直接催化不对称曼尼希型反应。手性路易斯酸/胺碱/布朗斯台德酸的组合用于催化将γ-丁烯内酯向N-二苯基膦酰基亚胺的γ加成反应,从而使产物收率最高> 99%,抗/ syn => 97:3,并且84%ee。除La(OTf)(3)/ Me-PyBox / TMEDA外,还使用催化量的TfOH对于提高产率和立体选择性很重要。

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