化学
环戊烷类
烯丙基重排
阳离子聚合
二烯
烯类反应
催化作用
共轭体系
药物化学
双键
有机化学
立体化学
天然橡胶
聚合物
摘要
C−H activation followed by addition to alkenes is challenging in the current C−H activation/functionalization field. We report herein an unprecedented diene-assisted transition-metal-catalyzed activation of allylic C−H bonds and their subsequent insertion into the alkene moieties of conjugated dienes. This novel C−H activation/alkene insertion reaction provides an efficient way to synthesize polysubstituted tetrahydropyrroles, tetrahydrofurans, and cyclopentanes with quaternary carbon centers. Preliminary mechanistic studies using D-labeling experiments have revealed that allylic C−H activation and alkene insertion are reversible steps, whereas the reductive elimination step, which is the final and the rate-determining step of the catalytic cycle, is irreversible.
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