化工时刊2024,Vol.38Issue(6) :40-46.DOI:10.16597/j.cnki.issn.1002-154x.2024.06.008

葫芦[8]脲催化光诱导[2+2]环加成反应的研究进展

Research Progress on Cucurbit[8]Uril-Catalyzed Photoinduced[2+2]Cycloaddition Reaction

张丽彦 张曙
化工时刊2024,Vol.38Issue(6) :40-46.DOI:10.16597/j.cnki.issn.1002-154x.2024.06.008

葫芦[8]脲催化光诱导[2+2]环加成反应的研究进展

Research Progress on Cucurbit[8]Uril-Catalyzed Photoinduced[2+2]Cycloaddition Reaction

张丽彦 1张曙1
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作者信息

  • 1. 东南大学化学化工学院,南京 211189
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摘要

光诱导[2+2]环加成反应是有机教科书中的一个经典反应,能够一步构建两个新的C—C键,生成含4个立体中心的高张力环丁烷化合物.近年来,大量研究表明葫芦[8]脲作为一种独特的大环化合物,在光诱导[2+2]环加成反应中展现出优异的催化性能.葫芦[8]脲不仅提高了[2+2]环加成反应的反应速率和转化率,并且因其空腔结构能选择性地结合客体分子从而控制反应底物的空间排列,使得反应具有立体选择性.作者综述了葫芦[8]脲在催化光诱导[2+2]环加成反应中的研究进展,并揭示了主客体相互作用在控制化学反应路径和产物选择性方面的巨大潜力.

Abstract

The photoinduced[2+2]cycloaddition reaction is a classic reaction in organic chemistry textbooks.It can construct two new C—C bonds in one step,generating high-tension cyclobutane compounds containing four stereocentres.In recent years,a number of studies have demonstrated that cucurbit[8]uril,a distinctive macrocyclic compound,exhibits remarkable catalytic performance in photoinduced[2+2]cycloaddition reactions.Cucurbit[8]uril not only enhances the rate and extent of photoinduced[2+2]cycloaddition reaction,but also controls the spatial arrangement of the reaction substrates due to its cavity structure,which enables the selective binding of guest molecules,thereby rendering the reaction stereoselective.This article presents a summary of the research progress made in the field of catalytic photoinduced[2+2]cycloaddition reactions using cucurbit[8]uril.It also discusses the potential of host-guest interactions in controlling chemical reaction pathways and product selectivity.

关键词

超分子化学/葫芦[8]脲/[2+2]环加成

Key words

supramolecular chemistry/cucurbit[8]uril/photoinduced[2+2]cycloaddition

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出版年

2024
化工时刊
东南大学

化工时刊

影响因子:0.333
ISSN:1002-154X
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