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- W2015374493 abstract "N-Iodosuccinimide (NIS) is a well-known iodination reagent that has found many applications in organic synthesis since it was first reported by Bunge. [1] [2] It is a colorless, stable solid, commercially available, and is widely used in organic transformations. It can be applied for iodination of arenes, [3] [4] halodecarboxylation, [5] [6] iodolysis of the Si-C bond, [7] [8] and chemoselective cleavage of silyl ethers. [9] Recent reports employ NIS in ring-opening reactions [10] or electrophilic cyclizations to yield substituted furans [11] and isoxazolidines. [12] Some of the examples reported in this article have roots in earlier reactions that have already been reviewed. [13]" @default.
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- W2015374493 date "2006-03-14" @default.
- W2015374493 modified "2023-10-05" @default.
- W2015374493 title "<i>N</i>-Iodosuccinimide (NIS)" @default.
- W2015374493 doi "https://doi.org/10.1055/s-2006-939055" @default.
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