5394-13-8, Chemical Research Letters, May 2021. Reactions catalyzed within inorganic and organic materials and at electrochemical interfaces commonly occur at high coverage, causing turnover rates to depend strongly on interfacial structure. In a article, 5394-13-8, molcular formula is C8H5BrS, introducing its new discovery.
Transition-metal-catalyzed coupling reactions are useful tools for synthesizing aryl sulfur compounds. However, conventional transition-metal-catalyzed thiolation of aryl bromides and chlorides typically requires the use of strong base under elevated reaction temperature. Herein, we report the first examples of nickel-catalyzed electrochemical thiolation of aryl bromides and chlorides in the absence of an external base at room temperature using undivided electrochemical cells.
5394-13-8, Interested yet? Read on for other articles about 5394-13-8!
Reference：
Benzothiophene – Wikipedia,
Benzothiophene | C8H6S – PubChem