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Enantioselective Rh(I)-Catalyzed C–H Arylation of Ferroceneformaldehydes
datasetposted on 2023-09-28, 18:36 authored by Chen-Xu Liu, Fangnuo Zhao, Qing Gu, Shu-Li You
As an important class of platform molecules, planar chiral ferrocene carbonyl compounds could be transformed into various functional groups offering facile synthesis of chiral ligands and catalysts. However, developing efficient and straightforward methods for accessing enantiopure planar chiral ferrocene carbonyl compounds, especially ferroceneformaldehydes, remains highly challenging. Herein, we report a rhodium(I)/phosphoramidite-catalyzed enantioselective C–H bond arylation of ferroceneformaldehydes. Readily available aryl halides such as aryl iodides, aryl bromides, and even aryl chlorides are suitable coupling partners in this transformation, leading to a series of planar chiral ferroceneformaldehydes in good yields and excellent enantioselectivity (up to 83% yield and >99% ee). The aldehyde group could be transformed into diverse functional groups smoothly, and enantiopure Ugi’s amine and PPFA analogues could be synthesized efficiently. The latter was found to be a highly efficient ligand in Pd-catalyzed asymmetric allylic alkylation reactions. Mechanistic experiments supported the formation of imine intermediates as the key step during the reaction.
suitable coupling partnersremains highly challengingppfa analogues couldmechanistic experiments supportedenantiopure ugi ’aldehyde group couldhighly efficient ligandeven aryl chloridesplanar chiral ferroceneformaldehydesdeveloping efficientchiral ligandsaryl iodidesaryl bromidessynthesized efficientlystraightforward methodsrhodium (platform moleculeskey stepimportant classimine intermediatesgood yieldsexcellent enantioselectivityespecially ferroceneformaldehydesenantioselective rhee ).)/ phosphoramidite