A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, Recommanded Product: 4-Cyanoindole, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 16136-52-0, Name is 4-Cyanoindole, molecular formula is C9H6N2. In a Article, authors is Schoemberg, Fritz£¬once mentioned of 16136-52-0
C-H Functionalization of Benzothiazoles via Thiazol-2-yl-phosphonium Intermediates
Benzothiazoles undergo regioselective C2-H functionalization with triphenylphosphine to form thiazol-2-yl-triphenylphosphonium salts, and these phosphonium salts react with a wide range of O- A nd N-centered nucleophiles to give the corresponding ethers, amines, and C-N biaryls. The reactions proceed under mild conditions and allow for the recovery of triphenylphosphine at the end of the sequence. In the presence of hydroxide, phosphonium salts undergo disproportionation, resulting in the reduction of the benzothiazole, which is useful for specific C2 deuteration of benzothiazoles.
Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. I hope my blog about is helpful to your research. Recommanded Product: 4-Cyanoindole
Reference£º
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