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Stereoselective Synthesis of P-C-S Pincer Ligand Coordinated Palladium Complexes by Alkoxypalladation of Chiral Ferrocenylphosphaalkenes

机译:对P-C-S钳子配体的立体选择性合成Chiral Ferrocenylphysalsalspalapalation alcoplapAldium钯配体

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The chemistry of pincer-complexes has attracted a considerable attention from organic and inorganic chemists because of the interesting reactivity and structural properties. As mentioned above, pincer-complexes proved to be versatile catalyst in organic transformations. Recently, we developed a novel method for the stereoselective synthesis of P-C-N pincer-palladium complexes la and lb containing a phospha-palladacyclopropane, in which the stereochemistry was controlled by the chiral ferrocene moiety. However, these complexes did not show the singnificant catalytic activities. Here, we report the synthesis of new P-C-S pincer complexes derived from the ferrocenylphosphaalkenes bearing an α-ferrocenyl sulfur atom substituent.
机译:由于有趣的反应性和结构性,夹冬冬络合物的化学吸引了来自有机和无机化学家的相当大的关注。如上所述,钳子复合物证明是有机转化中的通络催化剂。最近,我们开发了一种新的含有磷钯丙烷的P-C-N磷酸钯 - 络合物La和LB的新方法,其中通过手性二茂丙烷部分控制了立体化学。然而,这些配合物没有显示出单一的催化活性。在这里,我们报告了衍生自含有α-二茂烷基硫原子取代基的铁烯基膦烯烃的新的P-C-S钳子复合物的合成。

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