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 >First catalytic enantioselective synthesis of P-stereogenic phosphoramides via kinetic resolution promoted by a chiral bicyclic imidazole nucleophilic catalyst
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First catalytic enantioselective synthesis of P-stereogenic phosphoramides via kinetic resolution promoted by a chiral bicyclic imidazole nucleophilic catalyst

机译:通过手性双环咪唑亲核催化剂促进的动力学拆分,对P-立体异构磷酰胺进行催化对映选择性合成

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摘要

A novel method toward the synthesis of P-stereogenic organophosphorus compounds via kinetic resolution by a catalytic asymmetric phosphorylation through P-N bond formation has been developed. Using a chiral bicyclic imidazole nucleophilic catalyst, chiral phosphoramide compounds were prepared in high conversions and with moderate enantioselectivity. This is also the first example of the catalytic asymmetric synthesis of chiral phosphoramide compounds.
机译:已开发出一种新的方法,该方法通过通过P-N键形成的催化不对称磷酸化的动力学拆分来合成P-立体异构有机磷化合物。使用手性双环咪唑亲核催化剂,可以高转化率和中等对映选择性制备手性磷酰胺化合物。这也是手性磷酰胺化合物催化不对称合成的第一个例子。

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