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Synthesis of Chiral Aziridines through Decarboxylative Generation of Sulfur Ylides and their Reaction with Chiral Sulfinyl Imines

机译:硫叶立德的脱羧合成手性氮丙啶及其与手性亚磺酰基亚胺的反应

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摘要

Reaction of sulfur ylide with a series of aryl substituted chiral non-racemic sulfinyl imines afforded the corresponding aziridines in high yield and good stereoselection. The sulfur ylides were generated by the thermally induced decarboxylation of carboxymethylsulfonium betaines. A drop in the diastereomeric ratio was observed when going from electron deficient to electron releasing aryl substituted imines. Sulfonium methylidene aziridinations involving the decarboxylation of carboxymethylsulfonium betaine functionality compliments existing technologies with the advantages of the reaction protocol, levels of conversion and scope.
机译:硫叶立德与一系列芳基取代的手性非外消旋亚砜亚胺的反应以高收率和良好的立体选择得到了相应的氮丙啶。硫化氢是通过羧甲基be甜菜碱的热诱导脱羧反应生成的。当从缺乏电子的电子转变为释放电子的芳基取代的亚胺时,观察到非对映异构体比率下降。涉及羧甲基ulf甜菜碱官能团脱羧的methyl亚甲基叠氮化物使现有技术具有反应方案,转化水平和范围的优点。

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