Abstract
The reactions of 2-amino-8-hydroxyquinoline and 2-amino-4(1H)quinolone with different sulfonyl chlorides have been investigated. The chemoselectivity was observed to afford exclusively the arylsulfonate ester derivatives. The mechanism of the reaction is also discussed.
ACKNOWLEDGMENTS
This work was supported by grants from the Brazilian agency Coordination for the Improvement of Higher Education Service (CAPES) and from DAAD (German Academic Exchange Service).