With the hypothesis of simple units integration to create new reactivities,a strategy for the synthesis of polyfunctionalized 5-alkenyl-3-carbonylfurans fromγ-hydroxyl enal and 1,3-dicarbonyl compounds is established...With the hypothesis of simple units integration to create new reactivities,a strategy for the synthesis of polyfunctionalized 5-alkenyl-3-carbonylfurans fromγ-hydroxyl enal and 1,3-dicarbonyl compounds is established,featuring readily available starting materials,high efficiency,good functional groups compatibility,green chemistry with high atom economy and only water release,etc.,to provide a series of polyfunctionalized 5-alkenyl-3-carbonylfurans,which could be applied to the late-stage functionalization of naturally occurring compounds and bioactive molecules,as well as the transformation to pyrroles and polycyclic aromatic hydrocarbon via electrocyclic reaction.Theγ-hydroxyl has played an important role in the unexpected process of ring opening isomerization of 2H-pyran to furanones,as confirmed by detailed mechanistic studies.展开更多
基金Financial support from National Natural Science Foundation of China(Grant No.22201187)the starting grant from Capital Medical University(Grant No.3100-12400123)。
文摘With the hypothesis of simple units integration to create new reactivities,a strategy for the synthesis of polyfunctionalized 5-alkenyl-3-carbonylfurans fromγ-hydroxyl enal and 1,3-dicarbonyl compounds is established,featuring readily available starting materials,high efficiency,good functional groups compatibility,green chemistry with high atom economy and only water release,etc.,to provide a series of polyfunctionalized 5-alkenyl-3-carbonylfurans,which could be applied to the late-stage functionalization of naturally occurring compounds and bioactive molecules,as well as the transformation to pyrroles and polycyclic aromatic hydrocarbon via electrocyclic reaction.Theγ-hydroxyl has played an important role in the unexpected process of ring opening isomerization of 2H-pyran to furanones,as confirmed by detailed mechanistic studies.
