Jean-Michel BechtAlain WagnerCharles Mioskowski2012-11-152025-02-172012-11-152012-11-14https://dl.ftveti.edu.et/handle/123456789/4113Herein, we describe a mild and efficient two-step procedure to introduce a thiol group on aromatic substrates. First, reaction with an activated sulfoxide leads to an arylsulfonium salt intermediate. Then, two successive â- elimination-based dealkylation reactions afford the desired arylthiols in good to excellent yieldsHerein, we describe a mild and efficient two-step procedure to introduce a thiol group on aromatic substrates. First, reaction with an activated sulfoxide leads to an arylsulfonium salt intermediate. Then, two successive â- elimination-based dealkylation reactions afford the desired arylthiols in good to excellent yieldsenFacile Introduction of SH Group on Aromatic Substrates via Electrophilic Substitution ReactionsArticle