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首页> 外文期刊>Russian Journal of General Chemistry >Reactions of P(III) Chlorides with Aldehydes: I. Synthesis of Primary Intermediates of the Reactions of Aliphatic Aldehydes with P(III) Chlorides Possessing Electrophilic Properties
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Reactions of P(III) Chlorides with Aldehydes: I. Synthesis of Primary Intermediates of the Reactions of Aliphatic Aldehydes with P(III) Chlorides Possessing Electrophilic Properties

机译:P(III)氯化物与醛的反应:I.具有亲电性质的脂肪族醛与P(III)氯化物反应的主要中间体的合成

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摘要

An approach to investigation of reactions of electrophilic P(III) chlorides with aliphatic aldehydes is developed. Its essence is the removal of HC1 impurity from chloride and catalytic blocking of electrophilic center of the carbonyl group. For these purposes nitrogen-containing organic bases and alkyl vinyl ethers are used. Three types of primary intermediates with the nearest P(III) environment POCl2, O2PCl, and O3P are synthesized. It is established that the stability of intermediates increases with the growing acceptor properties of substituents at P(III) and donor properties of the aldehyde fragment.
机译:开发了一种研究亲电P(III)氯化物与脂族醛反应的方法。其实质是从氯化物中除去HCl杂质并催化封堵羰基的亲电子中心。为了这些目的,使用了含氮有机碱和烷基乙烯基醚。合成了三种具有最接近P(III)环境POCl2,O2PC1和O3P的主要中间体。可以确定的是,中间体的稳定性随P(III)上取代基的受体性质和醛片段供体性质的增长而增加。

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