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Structure-activity relationship studies of cyclopropenimines as enantioselective Bronsted base catalysts

机译:环丙亚胺作为对映选择性布朗斯台德碱催化剂的构效关系研究

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摘要

We recently demonstrated that chiral cyclopropenimines are viable Bronsted base catalysts in enantioselective Michael and Mannich reactions. Herein, we describe a series of structure-activity relationship studies that provide an enhanced understanding of the effectiveness of certain cyclopropenimines as enantioselective Bronsted base catalysts. These studies underscore the crucial importance of dicyclohexylamino substituents in mediating both reaction rate and enantioselectivity. In addition, an unusual catalyst CH...O interaction, which provides both ground state and transition state organization, is discussed. Cyclopropenimine stability studies have led to the identification of new catalysts with greatly improved stability. Finally, additional demonstrations of substrate scope and current limitations are provided herein.
机译:我们最近证明,手性环丙亚胺在对映选择性迈克尔和曼尼希反应中是可行的布朗斯台德碱催化剂。本文中,我们描述了一系列结构-活性关系研究,这些研究提供了对某些环丙炔亚胺作为对映选择性布朗斯台德碱催化剂有效性的增强理解。这些研究强调了二环己基氨基取代基在介导反应速率和对映选择性方面的至关重要性。此外,讨论了不寻常的催化剂CH ... O相互作用,它既提供基态又提供过渡态的组织。环丙亚胺的稳定性研究已导致鉴定出稳定性大大提高的新型催化剂。最后,本文提供了基板范围和电流限制的其他说明。

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