Abstract

A direct and efficient palladium-catalyzed desulfonylative carbonylation reaction for the synthesis of 3-arylquinoin-2(1H)-ones has been disclosed. The reaction proceeds with a rapid elimination of SO2 process by employing benzylsulfonyl chlorides as effective C(sp3) electrophiles, with anthranils as the N-source, a variety of 3-arylquinoin-2(1H)-ones were obtained in moderate to high yields. This protocol provides a good supplement for applying benzylsulfonyl chlorides as C(sp3) electrophiles in carbonylation reactions.

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