化学
环丙烷
烷基
激进的
戒指(化学)
基质(水族馆)
范围(计算机科学)
联轴节(管道)
组合化学
有机化学
拉伤
立体化学
环应变
药物化学
化学合成
催化作用
反应条件
还原消去
继电器
作者
Luyao Liu,Yongfang Yang,Shimin Jiang,Yameng Qin,Yu Hu,Xiaojun Zeng
出处
期刊:Organic Letters
[American Chemical Society]
日期:2026-09-07
卷期号:28 (37): 11582-11587
标识
DOI:10.1021/acs.orglett.6c03213
摘要
Abstract We report a nickel-catalyzed alkyl–alkyl cross-electrophile coupling of N-chlorocyclopropamides with tertiary alkyl bromides. This method leverages cyclopropane strain release to generate alkyl radicals via β-scission of nitrogen-centered radicals, enabling efficient C(sp3)–C(sp3) bond formation under mild reductive conditions. The protocol exhibits a broad substrate scope and excellent functional-group tolerance, affording diverse aliphatic products in good to excellent yields. Mechanistic studies support a radical relay pathway driven by strain-release ring opening and nickel-mediated cross-coupling. This strategy provides a modular, practical approach to complex aliphatic frameworks, expanding the utility of strain-release chemistry in cross-electrophile coupling.
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