反应性(心理学)
环加成
光化学
化学
接受者
自由基离子
药物化学
有机化学
催化作用
离子
医学
凝聚态物理
物理
病理
替代医学
作者
Soumitra Maity,Subhashis Mondal,Saradindu Debnath,Rabindranath Lo
标识
DOI:10.1002/anie.202419426
摘要
Altering the reactivity model of a molecule can potentially eliminate limitations existing in its current paradigm. When it comes to the activation of Donor-Acceptor Cyclopropanes (DACs), Lewis acids have been the state-of-the-art. Although a variety of polarized 2π components have been successfully coupled with DACs for [3+2] cycloaddition, unpolarized alkenes prove to be a roadblock due to an inherent polarity mismatch with the Lewis acid-mediated 1,3-zwitterionic intermediate. Hereby, harnessing the distonic radical cation mode of cleavage by photoredox catalysis overcomes this mismatched reactivity of the zwitterionic intermediate, providing a unique route to highly substituted cyclopentanes and cyclopentenes. Expansion of this strategy to bicyclo[1.1.0]butanes enables access to bicyclo[3.1.1]heptanes (BCHs) through a facile [3σ+2σ] cycloaddition. Detailed mechanistic insights are also provided using dispersion-corrected density functional theory.
科研通智能强力驱动
Strongly Powered by AbleSci AI