Because a catalyst decreases the height of the energy barrier, 25594-62-1, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.25594-62-1, Name is 2-Acetylquinoxaline, molecular formula is C10H8N2O. In a article£¬once mentioned of 25594-62-1
Asymmetric Michael Addition of 2-Acetyl Azaarenes to beta-CF3-beta-(3-indolyl)nitroalkenes Catalyzed by a Cobalt(II)/(imidazoline-oxazoline) Complex
The first enantioselective Michael addition of 2-acetyl azaarenes to beta-CF3-beta-(3-indolyl)nitroalkenes has been successfully achieved in the presence of a Co(II)/(imidazoline-oxazoline) complex as the catalyst. The reaction affords a series of CF3- A nd 3-indole-containing adducts featuring a trifluoromethylated all-carbon quaternary stereocenter in good to excellent yields (up to 99%) and enantioselectivities (up to 96% ee). Furthermore, the functional groups in the adducts including Ca?O, NO2, and the azaarene provide a large variety of useful transformations, leading to the formation of valuable intermediates such as optically active secondary alcohol, pyrroline, ester, and pyrrolidinone which all contain a 3-substituted indole and a trifluoromethylated all-carbon quaternary stereocenter.
A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. 25594-62-1, In my other articles, you can also check out more blogs about 25594-62-1
Reference£º
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N761 | ChemSpider