化学
烯丙基重排
克莱森重排
铑
催化作用
电泳剂
串联
对映选择合成
不对称诱导
有机化学
基质(水族馆)
筑地反应
芳基
立体化学
烷基
组合化学
复合材料
材料科学
地质学
海洋学
作者
Hu-Chong Wang,Ting-Jia Sun,Ziqi Yang,Qing Gu,Shu‐Li You
摘要
Transition metal-catalyzed asymmetric allylic dearomatization of β-naphthols provides efficient access to enantioenriched naphthalenones. However, these reactions generally suffer from limited substrate scope, incompatibility with alkyl-substituted allylic electrophiles, and poor understandings of the reaction mechanism. Herein, we report a rhodium-catalyzed asymmetric allylic dearomatization of β-naphthols utilizing a bisdihydrobenzooxaphosphole (BIBOP) chiral ligand. This catalytic system displays high yields and enantioselectivity and broad substrate scope, efficiently accommodating both alkyl- and aryl-substituted allylic carbonates. Detailed mechanistic studies reveal that the reaction proceeds through a tandem asymmetric allylic etherification/Claisen rearrangement sequence. This provides critical insights into the fundamental pathways for the asymmetric allylic dearomatization of naphthols.
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