Abstract:In this work, we present a rapid, metal‐free and efficient method for thiocyanation of aromatic amines under microwave irradiation for the synthesis of aryl thiocyanates using inexpensive and nontoxic NH4SCN as thiocyanato source and K2S2O8 as an oxidant. This protocol tolerates a wide range of substituted anilines to provide the corresponding thiocyanated products in good to excellent yields. The features of this strategy include a broad substrate scope, high functional group tolerance, mild reaction conditio… Show more
Aryl thiocyanate compounds play a crucial role as building blocks in the synthesis of bioactive compounds and intermediates for various functional groups. Here, we developed a highly efficient and novel...
Aryl thiocyanate compounds play a crucial role as building blocks in the synthesis of bioactive compounds and intermediates for various functional groups. Here, we developed a highly efficient and novel...
A photoinduced FeCl3/HCl synergistic catalytic method enables C(sp3)–S bond formation via reductive cross-coupling of activated/inert C(sp3)–H and aryl/alkyl sulfonyl chlorides through ligand-to-metal charge transfer (LMCT).
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