《Al(OTf)3-Catalyzed Tandem Coupling Reaction between N,N-Disubstituted Aminomalonitriles and Substituted Arenes: a Synthesis of 1-Cyano-bisindolylmethane Analogues》 was published in Advanced Synthesis & Catalysis in 2020. These research results belong to Lei, Lin-Sheng; Wang, Bo-Wen; Jin, Da-Ping; Gao, Zhu-Peng; Huan-Liang; Wang, Shao-Hua; Xu, Xue-Tao; Zhang, Kun; Zhang, Xiao-Yun. Recommanded Product: 399-52-0 The article mentions the following:
A synthesis of 1-cyano-bisarylmethane analogs via an Al(OTf)3-catalyzed tandem coupling reaction between N,N-disubstituted aminomalonitriles and substituted arenes were developed. This method not only provided an alternative synthetic strategy for the synthesis of corresponding functional mols., but also enriches the volume of bisarylmethanes library to facilitate related functional studies. The experimental part of the paper was very detailed, including the reaction process of 5-Fluoro-1H-indole(cas: 399-52-0Recommanded Product: 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.Recommanded Product: 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