区域选择性
苯乙烯
催化作用
对映选择合成
化学
芳基
联轴节(管道)
基质(水族馆)
醇盐
反应性(心理学)
有机化学
偶联反应
立体异构
组合化学
衍生工具(金融)
化学合成
甲基丙烯酸酯
反应条件
苯乙烯氧化物
甲烷氧化偶联
作者
Xiaoyu Lu,Haoyu Dong,Jun-Long Zhang,Jin-Tao Tao,Si-Nan Liu,Yi-Mei Wu
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2026-01-16
卷期号:16 (3): 2417-2426
标识
DOI:10.1021/acscatal.5c07500
摘要
Organoboron compounds are universally recognized as highly valuable synthetic building blocks, while the Suzuki–Miyaura cross-coupling has firmly established itself as a reliable platform for C–C bond formation. These salient features have fostered its widespread application across medicinal chemistry and materials science. Herein, a nickel-catalyzed, exogenous base-free, enantioselective Suzuki–Miyaura-type coupling of styrene oxides with arylboronic acids is reported. This reaction demonstrates high regioselectivity and enantioselectivity, a broad substrate scope, versatility for the late-stage modifications of bioactive molecules, and capability for synthesizing chiral drug precursors. Additionally, aryl aziridines can be employed as alternative coupling partners. Mechanistic studies confirm a stereoconvergent pathway involving radical intermediates, with in situ-generated alkoxide anions acting as the essential base. This methodology provides a practical approach for synthesizing enantioenriched diaryl alcohols and amines, which are valuable structural skeletons in pharmaceuticals and natural products.
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