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Hydrogenolysis of compounds with sulfur atoms attached to aromatic rings such as benzenethiols, and aryl sulfides, disulfides, sulfoxides and sulfones takes place on refluxing with Raney nickel or nickel boride. Sulfur combines with nickel, and hydrogen replaces the sulfur-containing group. [Pg.914]

See other pages where Aryl sulfides hydrogenolysis is mentioned: [Pg.164] [Pg.219] [Pg.1512]