15211-31-1Relevant academic research and scientific papers
Lewis Acid-Catalyzed Nucleophilic Substitutions of Benzylic Alcohols with Sulfamides
Oda, Ryoga,Nakata, Kenya
, p. 295 - 301 (2021)
Nucleophilic substitutions of benzylic alcohols with sulfamides were achieved using an FeCl3 Lewis acid catalyst in MeNO2. It was necessary to adjust the reaction conditions to obtain efficient yields depending on the stability of the carbocation intermediates. The reaction could easily be performed, and it was revealed that a variety of diarylmethanols and benzylic alcohols were applicable to the reaction, irrespective of the type and position of the substituents. The sulfamide moieties were easily deprotected and converted into amine groups.
