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- W3046242561 abstract "A metal-catalyzed route was developed for the synthesis of 2,3-diiminoindolines in good to high yields with short reaction times. Cu-catalyzed electrophilic addition and ring-opening/rearrangement steps were proposed as being involved in this donor-acceptor metallo carbenoid formation reaction with benzo[c]isoxazoles. Furthermore, under Pd-catalyzed hydrogenation conditions, the resulting products could be transformed into 2,3-diaminoindoles in moderate to high yields." @default.
- W3046242561 created "2020-08-07" @default.
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- W3046242561 date "2020-09-01" @default.
- W3046242561 modified "2023-10-14" @default.
- W3046242561 title "Synthesis of 2,3-diiminoindolines and 2,3-diaminoindoles via copper-catalyzed donor-acceptor metallo carbenoid formation and hydrogenation reactions" @default.
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- W3046242561 doi "https://doi.org/10.1016/j.tetlet.2020.152314" @default.
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