Hydrous zinc halide-catalyzed aminosulfonation of hydrocarbons
Literature Information
Biswajit Kalita, Angus A. Lamar, Kenneth M. Nicholas
Benzylic and allylic hydrocarbons are selectively converted to the corresponding sulfonamides by a ZnBr2–H2O-catalyzed reaction with PhINTs; saturated adamantane is aminosulfonated at the tertiary C–H bond.
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![2,6-Di(thiophen-2-yl)dithieno[3,2-b:2',3'-d]thiophene structure 2,6-Di(thiophen-2-yl)dithieno[3,2-b:2',3'-d]thiophene structure](https://static.chemtradehub.com/structs/910/910788-24-8-5b70.webp)


![2,6-Bis({(2R)-2-[hydroxy(diphenyl)methyl]-1-pyrrolidinyl}methyl)-4-methylphenol structure 2,6-Bis({(2R)-2-[hydroxy(diphenyl)methyl]-1-pyrrolidinyl}methyl)-4-methylphenol structure](https://static.chemtradehub.com/structs/877/877395-58-9-70bf.webp)