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- W4366975254 endingPage "3657" @default.
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- W4366975254 abstract "A novel, low-cost method for the preparation of not easily accessible free 3-aminoindoles has been developed. This approach is based on a well-established reaction between indoles and nitrostyrene in the presence of phosphorous acid, which results in the formation of 4′-phenyl-4′H-spiro[indole-3,5′-isoxazoles]. The latter could be transformed to corresponding aminated indoles by reaction with hydrazine hydrate in good or excellent yields upon microwave-assisted heating." @default.
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- W4366975254 date "2023-04-23" @default.
- W4366975254 modified "2023-09-30" @default.
- W4366975254 title "A Two-Step Synthesis of Unprotected 3-Aminoindoles via Post Functionalization with Nitrostyrene" @default.
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- W4366975254 doi "https://doi.org/10.3390/molecules28093657" @default.
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