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When 4-aminophenylsulfonamide was treated with a less reactive halogenating reagent than NIS (e.g., NBS) at room temperature, halogenation of its aromatic ring at the 3 position occured. See:, T. Mirzadegan, T. Silva, (Roche Palo Alto LLC, Palo Alto, CA), US-A 7388111, 2008.
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For details, see the Supporting Information
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For details, see the Supporting Information.
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13Ca NMR spectroscopy was established previously and is cited in refs.a [6] and [7].
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2 (3 a) and NIS in deuterated ortho-dichlorobenzene were unsuccessful, which could be due to the poor solubility of the amide and NIS in the solvent
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2 (3 a) and NIS in deuterated ortho-dichlorobenzene were unsuccessful, which could be due to the poor solubility of the amide and NIS in the solvent.
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The addition of catalytic amounts of Galvinoxyl to the reaction system did not suppress the reaction completely
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The addition of catalytic amounts of Galvinoxyl to the reaction system did not suppress the reaction completely.
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