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- W2337214852 abstract "<i>N</i>,<i>N</i>-Dihalosulfonamides are important reagents for various organic transformations. Simplicity, efficiency, and a unique chemical behaviour make this class of compounds synthetically useful. <i>N</i>,<i>N</i>-Dibromo-<i>p</i>-toluenesulfonamide (TsNBr<sub>2</sub>) is an efficient source of electrophilic bromine, which, at the same time, also provides the nucleophilic sulfonamide counterpart to form a C–N bond. This reagent has also been found to be a suitable precursor of nitrene. These diverse properties led to the development of various important organic transformations under catalyst-free and relatively mild reaction conditions. However, the strong oxidizing nature of this reagent sometimes appears as a limitation for a desired functional group transformation. 1 Introduction 2 Cohalogenation of Olefins 3 Activation of Alkynes with TsNBr<sub>2</sub> 4 Oxidation Reactions 5 Nitrene Transfer Reactions 6 Hofmann Rearrangement Using TsNBr<sub>2</sub> 7 Bromination of Aromatic Compounds 8 Cleavage of Oximes 9 Miscellaneous Reactions 10 Conclusion" @default.
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- W2337214852 date "2016-04-14" @default.
- W2337214852 modified "2023-10-03" @default.
- W2337214852 title "N,N-Dibromo-p-Toluenesulfonamide (TsNBr2): A Promising Alternative Bromo-Organic Reagent" @default.
- W2337214852 doi "https://doi.org/10.1055/s-0035-1562024" @default.
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