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alpha-Amido Sulfones as Stable Precursors of Reactive N-Acylimino Derivatives

机译:α-酰胺基砜作为稳定的反应性N-Acylimino衍生物的前体

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摘要

Nucleophilic addition to carbon-nitrogen double bonds is one of the most practiced methods for the synthesis of nitrogen derivatives.In terms of reactivity,a logical comparison with the carbonyl group immediately evidences a lower electrophilicity of the azomethine carbon that introduces several limitations in the utilization of these unsaturated derivatives.The most serious side process that often occurs working with C=X derivatives is a competitive enolization that definitively hampers any efficient addition.To overcome this problem,various synthetic efforts have been done as the development of new nucleophilic systems was endowed with a consistent reactivity but featured by a low basicity.Organo-cerium,alkyl cuprates,and other allyl-based orga-nometallic reagents have been successfully used with a variety of imino derivatives.
机译:碳氮双键的亲核加成是合成氮衍生物最常用的方法之一。就反应性而言,与羰基的逻辑比较立即证明,偶氮甲碱碳的亲电子性较低,这在使用中引入了一些限制与这些不饱和衍生物一起使用最常见的最严重的副反应是竞争性烯醇化。它最终会阻碍任何有效的加成反应。为克服这一问题,随着新亲核体系的发展,人们进行了各种合成努力具有一致的反应性,但具有较低的碱度。有机铈,烷基铜酸盐和其他基于烯丙基的有机金属非金属试剂已成功用于各种亚氨基衍生物。

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