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• W2012505591 abstract "Radical carboiodination of various aryl amines is reported. Aryl diazonium salts, generated in situ from the corresponding aryl amines, are reacted with Bu4NI to provide the corresponding aryl radicals which undergo 5-exo or 6-exo cyclization. Iodine abstraction eventually affords the carboiodinated products in good to excellent yields. If TEMPO is added, the cascade provides the cyclized carboaminoxylation products. Running the reaction in the presence of PhTeTePh affords the phenyltellurated cyclized products." @default.
• W2012505591 created "2016-06-24" @default.
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• W2012505591 date "2014-07-07" @default.
• W2012505591 modified "2023-09-27" @default.
• W2012505591 title "Cyclizing Radical Carboiodination, Carbotelluration, and Carboaminoxylation of Aryl Amines" @default.
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• W2012505591 doi "https://doi.org/10.1002/anie.201403968" @default.
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