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1,3-Dithianes as Acyl Anion Equivalents in Pd-Catalyzed Asymmetric Allylic Substitution

机译:Pd催化的不对称烯丙基取代基中的1,3-二乙胺为酰基阴离子当量

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摘要

A Pd-catalyzed asymmetric allylic substitution with 1,3-dithianes as acyl anion equivalents has been developed in high yields and excellent enantioselectivities. The reaction was performed on a gram scale, and the corresponding alkylated products were conveniently converted into several biologically active products. This work provides an alternative strategy utilizing electrophilic carbonyl compounds as nucleophilic species in a Pd-catalyzed allylic substitution.
机译:已开发出高产率和出色的对映选择性的Pd催化的1,3-二硫醚类作为酰基阴离子当量的不对称烯丙基取代基。该反应以克为单位进行,并且相应的烷基化产物方便地转化为几种生物活性产物。这项工作提供了一种替代策略,利用亲电羰基化合物作为Pd催化的烯丙基取代中的亲核物种。

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