Hydrous zinc halide-catalyzed aminosulfonation of hydrocarbons
Chemical Communications2008Iss. 36, pp. 4291–4291
Citations Over TimeTop 18% of 2008 papers
Abstract
Benzylic and allylic hydrocarbons are selectively converted to the corresponding sulfonamides by a ZnBr2-H2O-catalyzed reaction with PhI=NTs; saturated adamantane is aminosulfonated at the tertiary C-H bond.
Related Papers
- → Transition metal-catalyzed allylic substitution reactions with unactivated allylic substrates(2015)668 cited
- → Metal-catalyzed rearrangements of allylic esters(1984)59 cited
- → One-Pot Synthesis of Homoallylic Alcohols via a Facile Conversion of Allylic Alcohols into Allylic Iodides(1989)30 cited
- → Green and selective iodination of diamondoid adamantane by β-cyclodextrin as a molecular reactor(2019)7 cited