Palladium-catalyzed oxidative cycloaddition through C-H/N-H activation: access to benzazepines was written by Wang, Lei;Huang, Jiayao;Peng, Shiyong;Liu, Hui;Jiang, Xuefeng;Wang, Jian. And the article was included in Angewandte Chemie, International Edition in 2013.Recommanded Product: 5-Isopropylindoline-2,3-dione This article mentions the following:
A synthesis of benzazepine heterocycles from isatins and alkynes via direct Pd-catalyzed oxidative cycloaddition is developed. Heterocycles are well tolerated in the reaction, which allows access to a number of unique mol. structures. The significance of the benzazepine scaffold as a structural element should render this method attractive for both synthetic and medicinal chem. In the experiment, the researchers used many compounds, for example, 5-Isopropylindoline-2,3-dione (cas: 150560-58-0Recommanded Product: 5-Isopropylindoline-2,3-dione).
5-Isopropylindoline-2,3-dione (cas: 150560-58-0) belongs to indole derivatives. Indole produced by Proteus, Pseudomonas, Escherichia and other species was shown to be a growth promoting factor in Arabidopsis thaliana. Indole plays a fundamental role for QS in E. coli, being one of the signal molecules responsible for the transcription of a variety of genes (gabT, and tnaB ASTD). Recommanded Product: 5-Isopropylindoline-2,3-dione
Referemce:
Indole alkaloid derivatives as building blocks of natural products from闂佽壈浜崹淇沜illus thuringiensis闂佽壈浜粋鍧闂佽壈浜崹淇沜illus velezensis闂佽壈浜粋鍧 their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles