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Asymmetric Synthesis of 1,2-Diamines bearing Tetrasubstituted Centers from Nonstabilized Azomethine Ylides and N-Sulfinylketimines under Bronsted Acid Catalysis

机译:在布朗斯台德酸催化下由不稳定的甲亚胺基叶立德油和N-亚磺酰基酮亚胺不对称合成带有四取代中心的1,2-二胺

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摘要

The first asymmetric cycloaddition of nonstabilized azomethine ylide and N-sulfinylimines is presented. In reactions with aryl-alkyl and heteroaryl-alkyl ketimines, excellent diastereoselectivities and good yields are obtained in all cases, regardless of the electronic character of the substituents at the aromatic rings. Moreover, the cycloadducts obtained can easily be deprotected in acid media, giving access to free 1,2-diamines which are prevalent in many natural and pharmaceutical products.
机译:提出了不稳定的偶氮甲碱叶立德和N-亚磺酰亚胺的第一次不对称环加成反应。在与芳基-烷基和杂芳基-烷基酮亚胺的反应中,不管芳环上取代基的电子特性如何,在所有情况下均获得优异的非对映选择性和良好的产率。而且,所获得的环加合物可以在酸性介质中容易地脱保护,从而获得在许多天然和药物产品中普遍存在的游离的1,2-二胺。

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