With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.51417-51-7,7-Bromoindole,as a common compound, the synthetic route is as follows.
51417-51-7, General procedure: To a 10 mL flame-dried Schlenk tube equipped with a stirring bar, indole1 (0.2 mmol), alpha-amido-sulfone 2 (0.2 mmol), and K2S2O8 (108.1mg, 0.4 mmol) were added. Toluene (1.2 mL) was injected into thetube at r.t. After stirring for 48 h, the mixture was purified by silica gelchromatography to afford the desired product 3.
As the paragraph descriping shows that 51417-51-7 is playing an increasingly important role.
Reference£º
Article; Wu, Xiaoyan; Xue, Lu; Luo, Shilong; Jia, Shiqi; Ao, Jun; Qin, Wenling; Synthesis; vol. 49; 22; (2017); p. 5017 – 5024;,
Indole alkaloid derivatives as building blocks of natural products from?Bacillus thuringiensis?and?Bacillus velezensis?and their antibacterial and antifungal activity study
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