A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, Recommanded Product: 5-Iodo-1H-indole, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 16066-91-4, Name is 5-Iodo-1H-indole, molecular formula is C8H6IN. In a Article, authors is Tarasenko, Elena A.£¬once mentioned of 16066-91-4
Enantioselective Copper(II)/Box-Catalyzed Synthesis of Chiral beta3-Tryptophan Derivatives
beta-Amino acids and their derivatives are important building blocks for the preparation of various bioactive compounds and materials. We developed a highly efficient method for the synthesis of beta3-tryptophan derivatives based on enantioselective Friedel-Crafts alkylation of indoles with phthaloyl-protected aminomethylenemalonate in the presence of chiral Cu(OTf)2/iPrBox complex as a catalyst. A wide range of indoles with electron-donating and electron-withdrawing substituents gave the desired products in high yields (up to 99 %) and excellent enantioselectivities (up to 99 % ee). In the case of pyrrole the Friedel-Crafts product was obtained in up to 90 % yield and up to 82 % ee.
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: 5-Iodo-1H-indole
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