Publication: DBU-Mediated Reaction of 3-Chlorooxindole and 9-Xanthyl Fluorene for Synthesis of 3-Arylidene Oxindole
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Abstract
This work reports a new route for the synthesis of 3-(9H-fluoren-9-ylidene)indolin-2-one derivatives via the reaction of 3-chlorooxindoles and O-ethyl S-(9H-fluoren-9-yl) carbonodithioates mediated by 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU). The reactions readily proceeded at room temperature, enable a collection of 3-alkenyl oxindoles to be prepared within a short reaction time (15 minutes). The 3-alkenyl oxindoles can be easily converted to 3-fluorenyl oxindoles by NaBH4 reduction.
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3-Alkenyl-oxindoles, 3-Chloroindolin-2-one, cross-coupling, DBU, O-ethyl S-(9H-fluoren-9-yl) carbonodithioate
Citation
Asian Journal of Organic Chemistry, 14(4), 2025
