分子内力
化学
催化作用
亲核细胞
催化循环
环加成
炔烃
溶剂效应
密度泛函理论
组合化学
反应机理
计算化学
溶剂
机制(生物学)
药物化学
立体化学
亲核加成
光化学
质子
产品(数学)
产量(工程)
亲核取代
作者
Yugui Qiu,Zhenfeng Shang,Xiufang Xu
标识
DOI:10.1021/acs.joc.5c03218
摘要
The [3 + 2] cycloaddition mechanism of the rhodium-catalyzed redox-neutral cyclization of sulfoxonium ylides with 1,4-diphenyl-1,3-butadiyne has been investigated using density functional theory. The calculations indicate that the active catalyst is [Cp*Rh(OAc)2]. The reaction proceeds sequentially through C(sp2)-H bond cleavage, alkyne insertion into the Rh-C(sp2) bond, intramolecular nucleophilic addition, protodemetalation, and stepwise proton migration, ultimately affording the product 3-phenyl-2-(phenylethynyl)-1-indenone. Additionally, based on the computational results, we propose that the rate-determining step of the catalytic cycle is governed by both C-H activation and intramolecular nucleophilic addition, rather than being controlled by a single step alone.
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