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首页> 外文期刊>Russian Journal of General Chemistry >Synthesis of Optically Active α-Aminophosphine Oxides and Enantioselective Membrane Transport of Acids with Their Participation
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Synthesis of Optically Active α-Aminophosphine Oxides and Enantioselective Membrane Transport of Acids with Their Participation

机译:旋光性α-氨基膦氧化物的合成及酸的对映选择性膜转运及其参与

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摘要

Previously, we have shown the prospect of using lipophilic α-aminophosphine oxides in the processes of membrane extraction for efficient and selective extraction of substrates of different nature, including mineral and organic acids [1]. We first attempted to carry out the enantioselective membrane transport of chiral carboxylic acids with optically active α-aminophosphine oxides. For their synthesis we used the Kabachnik-Fields reaction in the three-component system phosphinous acid-formaldehyde-amine.
机译:以前,我们已经显示了在膜提取过程中使用亲脂性α-氨基膦氧化物的潜力,可以有效,选择性地提取不同性质的底物,包括无机酸和有机酸[1]。我们首先尝试用旋光性α-氨基膦氧化物进行手性羧酸的对映选择性膜运输。对于它们的合成,我们在三组分次膦酸-甲醛-胺体系中使用了Kabachnik-Fields反应。

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