Synthetic Route of 1215-59-4, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.1215-59-4, Name is 5-(Benzyloxy)-1H-indole, molecular formula is C15H13NO. In a Article£¬once mentioned of 1215-59-4
Chiral phosphoric acid catalyzed asymmetric Friedel-Crafts alkylation of indole with 3-hydroxyisoindolin-1-one: Enantioselective synthesis of 3-indolyl-substituted isoindolin-1-ones
Chiral phosphoric acids have been proven to be effective organocatalysts for the asymmetric Friedel-Crafts alkylation of indoles with 3-hydroxyisoindolin-1-ones. The corresponding products were obtained in excellent chemical yields (up to 99%) with moderate to excellent enantioselectivities (up to >99ee after a single recrystallization). This is the first example of the catalytic asymmetric synthesis of valuable 3-substituted isoindolin-1-ones in high yields and enantioselectivities.
The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 1215-59-4 is helpful to your research. Synthetic Route of 1215-59-4
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