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Stereocontrolled 1,3-dipolar cycloadditions using Oppolzer's camphor sultam as the chiral auxiliary for carbonyl stabilized azomethine ylides

机译:使用Oppolzer的樟脑sultam作为羰基稳定的偶氮甲碱的手性助剂,进行立体控制的1,3-偶极环加成反应

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摘要

Two complementary approaches to substituted pyrrolidines via stereocontrolled 1,3-dipolar cycloaddition reactions of chiral azomethine ylides are desctibed.In one approach,chiral azomethine ylides were generated by thermolysis of aziridine carboxylate sultams and trapped with a variety of dipolarophiles to give good yields of the corresponding cycloadducts.In the second approach,chiral azomethine ylides were generated from glycyl sultams by 'imine tautomerization' and trapped with dipolarophiles to give good yields of the corresponding cycloadducts.
机译:描述了两种通过手性偶氮甲啶基团的立体控制的1,3-偶极环加成反应取代吡咯烷的互补方法。一种方法是,通过手性氮丙啶羧酸酯阿马替尼的热解生成手性偶氮甲,并用多种偶极亲和剂捕获,得到良好的收率。在第二种方法中,通过“亚胺互变异构化”从甘氨酰阿耳中生成手性偶氮甲亚胺,并用双极性亲和剂捕获,得到相应环加合物的良好收率。

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