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首页> 外文期刊>Tetrahedron, Asymmetry: The International Journal for Repid Publication on all Aspects of Asymmetry in Orgainc, Inorganic, Organometallic, Physical and Bio-Organic Chemistry >Novel chiral bis(oxazolines): synthesis and application as ligands in the copper-catalyzed enantioselective conjugate addition of diethylzinc to enones
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Novel chiral bis(oxazolines): synthesis and application as ligands in the copper-catalyzed enantioselective conjugate addition of diethylzinc to enones

机译:新型手性双(恶唑啉):在铜催化的二乙基锌与烯酮的铜催化对映选择性共轭加成中的合成和配体应用

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摘要

Novel chiral C-2-symmetric bis(oxazolines) were prepared from tartaric acid. They were applied as ligands in the copper-catalyzed conjugate addition of diethylzinc to chalcone and 2-cyclohexenone. Maximum enantiomeric excesses of 50% and 53% were obtained, respectively. The sense of induction was found to depend on the configuration of the stereogenic centre in the oxazoline ring, and not on the stereogenic centres of the 1,4-dioxane backbone. (c) 2005 Elsevier Ltd. All rights reserved.
机译:由酒石酸制备新型手性C-2-对称双(恶唑啉)。它们作为配体应用于二乙基锌向查耳酮和2-环己烯酮的铜催化共轭加成中。获得的最大对映体过量分别为50%和53%。发现诱导的感觉取决于恶唑啉环中的立体中心的构型,而不取决于1,4-二恶烷骨架的立体中心。 (c)2005 Elsevier Ltd.保留所有权利。

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