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 >Enantioselective synthesis of planar-chiral 1,11-dioxa-[11]paracyclophane-derived phosphoramidites and their use as chiral ligands
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Enantioselective synthesis of planar-chiral 1,11-dioxa-[11]paracyclophane-derived phosphoramidites and their use as chiral ligands

机译:平面手性1,11-二恶英-[11]对环磷酰胺衍生的亚磷酰胺的对映选择性合成及其作为手性配体的用途

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摘要

A library of bench-stable planar-chiral 1,11-dioxa[11]paracyclophane-derived phosphoramidites was synthesized by a three step procedure: enantioselective ortho-lithiation, reductive amination and coupling with phosphorochloridites. The efficacy of these phosphoramidite as chiral ligands was tested in the Pd-catalyzed allylic alkylation of dimethyl malonate and the Cu-catalyzed ethylation of chalcone under the reported conditions, with moderate enantioselectivity being obtained. (C) 2016 Elsevier Ltd. All rights reserved.
机译:通过以下三个步骤合成了稳定的平面稳定的手性1,11-二恶英[11]对环磷酰胺衍生的亚磷酰胺库:对映选择性的原位锂化,还原胺化和与次氯酸盐的偶联。在报道的条件下,在丙二酸二甲酯的钯催化的烯丙基烷基化反应和查尔酮的铜催化的乙基化反应中,测试了这些亚磷酰胺作为手性配体的功效,获得了中等的对映选择性。 (C)2016 Elsevier Ltd.保留所有权利。

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