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Synthesis, structure determination, and (radio-)fluorination of novel functionalized phosphanes suitable for the traceless Staudinger ligation

机译:适用于无痕施陶丁格连接的新型功能化膦的合成,结构测定和(放射性)氟化

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摘要

An elegant and efficient synthesis approach for the preparation of novel benzoate and nicotinate containing phosphanes is presented. This reaction path has a broad substrate scope. Thus, various functionalized phosphanes were obtained in high yields using an esterification procedure under Steglich conditions. A facile blocking of the phosphorus atom with BH_3 was carried out. BH3 as easily insertable and removable protecting group enables a further derivatization of the benzoate residue. The prepared phosphane derivatives proved to be valuable labeling building blocks for the implementation of a bioorthogonal (radio-)fluorination strategy and were applied for labeling purposes using the traceless Staudinger ligation. For this purpose, a selection of azide-functionalized small organic and bioactive sample molecules was prepared. Furthermore, a mild and selective (radio-)fluorination of these derivatives is demonstrated adopting this bioorthogonal ligation method.
机译:提出了一种优雅而有效的合成方法,用于制备新型的含苯甲酸酯和烟酸酯的膦。该反应路径具有广泛的底物范围。因此,在Steglich条件下使用酯化方法以高收率获得了各种官能化的膦。用BH_3轻松封堵了磷原子。 BH3作为易于插入和除去的保护基,可以进一步衍生苯甲酸酯残基。所制备的膦衍生物被证明是实施生物正交(放射性)氟化策略的有价值的标记构建基块,并使用无痕施陶丁格连接法用于标记目的。为此,准备了一些叠氮化物官能化的有机和生物活性小分子样品。此外,采用这种生物正交连接方法证明了这些衍生物的轻度和选择性(放射性)氟化。

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