A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, Quality Control of: Methyl 5-methoxy-1H-indole-3-carboxylate, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 172595-68-5, Name is Methyl 5-methoxy-1H-indole-3-carboxylate, molecular formula is C11H11NO3. In a Article, authors is Cao, Trung，once mentioned of 172595-68-5
In this Article, a strategy to obtain highly enantioselective catalysts for the Claisen rearrangement of allyloxy-and propargyloxy-indoles is outlined. Ultimately, copper BOX and palladium BINAP or PHOX catalysts were discovered as superior in catalyzing Claisen rearrangements of allyloxy-or proparyloxy-substituted indoles to generate oxindoles bearing allyl-or allenyl-substituted quaternary centers. This method proved to be tolerant of a broad range of functional groups. Tandem reactions of the silyl-allene products provide rapid access to a variety of spirocyclic oxindoles in one operation.
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. Quality Control of: Methyl 5-methoxy-1H-indole-3-carboxylate
Reference：
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