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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 >Synthesis of [2.2]paracyclophane-based bidentate oxazoline-carbene ligands for the asymmetric 1,2-silylation of N-tosylaldimines
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Synthesis of [2.2]paracyclophane-based bidentate oxazoline-carbene ligands for the asymmetric 1,2-silylation of N-tosylaldimines

机译:基于基于截谱的基于比特基于N-Tosyldimines的非对称1,2-甲硅烷基化的基于基于比赛的二齿恶唑啉 - 卡唑啉 - 甲苯配体

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摘要

A series of novel oxazoline-substituted imidazolium salts with planar and central chirality has been successfully synthesized and applied to copper-catalyzed enantioselective 1,2-silylation of N-tosylaldimines. The oxazoline-carbene copper complex generated in situ by the reaction of the oxazoline-substituted imidazolium and Cu2O demonstrated an exceptionally high catalytic activity in the asymmetric 1,2-silylation of N-tosylaldimines, affording chiral alpha-amino silanes with excellent yields and enantioselectivities. (C) 2017 Elsevier Ltd. All rights reserved.
机译:已经成功地合成了一系列新的恶唑啉取代的咪唑鎓盐,并已成功地合成并应用于铜催化的N-甲硅烷基二氧化胺的铜催化的对映选择性1,2-甲硅烷基化。 通过恶唑啉 - 取代的咪唑鎓和Cu 2 O反应原位产生的恶唑啉 - 碳铜复合物在N-甲硅烷基二胺的不对称1,2-甲硅烷基化中表现出具有极高催化活性,得到手性α-氨基硅烷,具有优异的产率和对映射性 。 (c)2017 Elsevier Ltd.保留所有权利。

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