化学
环加成
有机催化
分子内力
催化作用
光催化
环丁烷
光化学
路易斯酸
氢键
组合化学
铱
基质(水族馆)
戒指(化学)
对映选择合成
有机化学
分子
地质学
海洋学
作者
Stefania Perulli,Om Desai,Sandra Ardevines,Mustafa Uygur,Samuel Delgado‐Hernández,Olga Garcı́a Mancheño
标识
DOI:10.1002/adsc.202301217
摘要
Abstract The combination of organocatalytic activation and photocatalysis for enabling the intramolecular [2+2]‐cycloaddition of enone‐ene substrates bearing one Lewis base binding site is reported. While in a variety of solvents a poor conversion or no reaction takes place in the absence of a hydrogen bonding catalyst, the corresponding ring‐fused cyclobutane products could be built in moderate to good yields using a synergistic dual iridium‐urea co‐catalytic system. Control and mechanistic studies supported the postulated interaction between the organocatalyst and the substrate, which proved essential for an efficient energy transfer from the photosensitizer.
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