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- W4307159968 abstract "Abstract Radical cation cycloadditions have long been known as unique reactions and yet are intensively studied chemical transformations in the field of modern synthetic organic chemistry. The key to developing new reactions of this class is the generation and control of highly reactive radical cation intermediates. Herein, we report TiO 2 photochemical [2+2] and [4+2] cycloadditions using aryl vinyl ethers as radical cation precursors. The constructions of various four‐ and six‐membered rings are made possible by these radical cation cycloadditions. Although detailed mechanistic aspects remain unclear, 2,3‐dimethyl‐1,3‐butadiene ( 3 ) is found to be more radicalophilic than 2‐ethyl‐1‐butene ( 2 ) and effectively traps the radical cation of the aryl vinyl ethers to construct six‐membered rings." @default.
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- W4307159968 date "2022-11-24" @default.
- W4307159968 modified "2023-10-16" @default.
- W4307159968 title "Photochemical Radical Cation Cycloadditions of Aryl Vinyl Ethers" @default.
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- W4307159968 doi "https://doi.org/10.1002/ejoc.202201207" @default.
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