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Fe-catalyzed thioesterification of carboxylic esters

机译:铁催化的羧酸酯的硫酯化

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摘要

Second nature: Starting from shelf-stable aryl esters and thiols, a variety of carboxylic acid esters were transformed into the corresponding thioesters with no racemization of labile stereocenters (see scheme). The method was successfully applied in a native chemical-ligation-type peptide formation, which suggests that the thiol may act as a co-catalyst for future 1,2-additions of pronucleophiles to carboxylic esters.
机译:第二性质:从稳定的芳基酯和硫醇开始,各种羧酸酯被转化为相应的硫酯,而没有外消旋的立体中心(见方案)。该方法已成功地应用于天然化学连接型肽的形成,这表明硫醇可能充当亲核试剂未来向羧酸酯中1,2-加成的助催化剂。

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