《Oxidative dearomative cross-dehydrogenative coupling of indoles with diverse C-H nucleophiles: efficient approach to 2,2-disubstituted indolin-3-ones》 was written by Yan, Xue; Tang, Ying-De; Jiang, Cheng-Shi; Liu, Xigong; Zhang, Hua. SDS of cas: 399-52-0 And the article was included in Molecules in 2020. The article conveys some information:
The oxidative, dearomative cross-dehydrogenative coupling of indoles with various C-H nucleophiles was developed. This process features a broad substrate scope with respect to both indoles and nucleophiles, affording structurally diverse 2,2-disubstituted indolin-3-ones in high yields (up to 99%). The oxidative dimerization and trimerization of indoles were demonstrated under the same conditions. In the experimental materials used by the author, we found 5-Fluoro-1H-indole(cas: 399-52-0SDS of cas: 399-52-0)
5-Fluoro-1H-indole(cas: 399-52-0) is a member of aromaticfluorinated building blocks. Fluorine-containing aromatics have been incorporated into crop-protection chemicals (herbicides, insecticides, fungicides). Liquid crystals, positron emission tomography, and imaging systems represent new areas where fluoroaromatics and fluoroheterocyclics have gained attention.SDS of cas: 399-52-0
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Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles