Reactions catalyzed within inorganic and organic materials and at electrochemical interfaces commonly occur at high coverage and in condensed media, causing turnover rates to depend strongly on interfacial structure and composition, 201530-41-8, Name is Deferasirox, SMILES is O=C(O)C1=CC=C(N2N=C(C3=CC=CC=C3O)N=C2C4=CC=CC=C4O)C=C1, in an article , author is Duan, Shengguo, once mentioned of 201530-41-8, Application In Synthesis of Deferasirox.
Acyloxy-substituted alpha,beta-unsaturated imines generated in situ from triazoles can act as aza-[4 C] synthons and be trapped by indoles in a stepwise [4 + 2] cycloaddition reaction, thus providing rapid access to valuable pyrido[2,3-b]indoles in high yields. Attractive features of this reaction system include operational simplicity, readily available substrates, construction of sterically demanding quaternary centers, and convenient derivatization using triflate.
But sometimes, even after several years of basic chemistry education, it is not easy to form a clear picture on how they govern reactivity! 201530-41-8, you can contact me at any time and look forward to more communication. Application In Synthesis of Deferasirox.
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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