Electric Literature of 1912-33-0, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 1912-33-0, Name is Methyl 2-(1H-indol-3-yl)acetate, molecular formula is C11H11NO2. In a Article，once mentioned of 1912-33-0
The bisindolesuccinic acid ester 8b was obtained as a mixture of diastereomers by iodine promoted coupling of the dianion 7b or via the trianion 7a.The diester was converted to the N-benzylimide 10 which was oxidatively cyclized to the indolo<2,3-a>pyrrolo<3,4-c>carbazole compound 13.
Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Electric Literature of 1912-33-0, you can also check out more blogs about1912-33-0
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