表面改性
黄素组
光催化
催化作用
化学
酚类
组合化学
有机催化
光化学
光催化
有机化学
对映选择合成
酶
物理化学
作者
Majid Ahmad Ganie,Niladri Sekhar Roy,Abdul Rauf Raza,Burkhard Koenig,Debayan Sarkar
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2025-09-26
卷期号:: 17078-17088
标识
DOI:10.1021/acscatal.5c05312
摘要
para-Quinone methides (p-QMs) are versatile, transient electrophilic dearomatized intermediates in organic synthesis, enabling a range of transformations, such as cycloadditions, nucleophilic additions, and cascade reactions. Conventionally, these ephemeral species are generated in situ via acid- or base-mediated activation of phenols prefunctionalized with a leaving group (e.g., hydroxyl, halide, or sulfonate) at the benzylic position or through oxidation of phenols employing toxic heavy metal salts (e.g., lead, silver, or bismuth). We report a photocatalytic approach for in situ generation of p-QMs directly from simple phenolic precursors, thereby circumventing the need for benzylic prefunctionalization or transition-metal reagents. The photogenerated p-QMs undergo efficient transformations, including benzylic functionalization, spirocyclization, and spiroepoxidation, delivering rapid access to benzylic scaffolds and structurally complex sp3-rich spirocyclic frameworks. The synthetic utility of this approach is further demonstrated by the late-stage functionalization of drugs and natural products.
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