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Scope and Mechanism on Iridium-f-Amphamide Catalyzed Asymmetric Hydrogenation of Ketones 被引量:4

Scope and Mechanism on Iridium-f-Amphamide Catalyzed Asymmetric Hydrogenation of Ketones
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摘要 A series of novel and easily accessed ferrocene-based amino-phosphine-sulfonamide (f-Amphamide) ligands have been developed and ap- plied in Ir-catalyzed asymmetric hydrogenation of aryl ketones, affording the corresponding chiral secondary alcohols with excellent results (up to 〉99% conversion, 〉99% ee and TON up to 200 000). DFT calculations suggest an activating model involving an alkali cation Li. A series of novel and easily accessed ferrocene-based amino-phosphine-sulfonamide (f-Amphamide) ligands have been developed and ap- plied in Ir-catalyzed asymmetric hydrogenation of aryl ketones, affording the corresponding chiral secondary alcohols with excellent results (up to 〉99% conversion, 〉99% ee and TON up to 200 000). DFT calculations suggest an activating model involving an alkali cation Li.
出处 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2018年第9期851-856,共6页 中国化学(英文版)
关键词 aryl ketone asymmetric f-Amphamide HYDROGENATION IRIDIUM aryl ketone asymmetric f-Amphamide hydrogenation iridium
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