Application of 148461-16-9, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.148461-16-9, Name is (S)-4-(tert-Butyl)-2-(2-(diphenylphosphino)phenyl)-4,5-dihydrooxazole, molecular formula is C25H26NOP. In a Article，once mentioned of 148461-16-9
A modular six-step asymmetric synthesis of two naturally occurring and three non-natural isoflavanones containing tertiary alpha-aryl carbonyls is reported. This synthetic route, utilising a Pd-catalyzed decarboxylative asymmetric protonation, produces isoflavanones in excellent enantioselectivities from 76-97 %. A switch in the sense of stereoinduction was observed when different H+ sources were employed, showing the first example of dual stereocontrol in an asymmetric protonation reaction. The first enantioselective synthesis of the naturally occurring isoflavanones sativanone and 3-o-methylviolanone has been accomplished. Proton haze – Don?t know if I?m comin’ up or down: The first asymmetric synthesis of the naturally occurring isoflavanones, sativanone and 3-O-methylviolanone, containing tertiary alpha-aryl carbonyls, has been accomplished. This was achieved through a Pd-catalyzed decarboxylative asymmetric protonation in excellent enantioselectivities from 76-97 %. A switch in the sense of stereoinduction was observed when different H+ sources were employed.
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 148461-16-9 is helpful to your research. Application of 148461-16-9
Reference：
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI