Application of 18514-76-6, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.18514-76-6, Name is 5-Nitroquinoxaline, molecular formula is C8H5N3O2. In a article，once mentioned of 18514-76-6
Ruthenium-Catalyzed Selective C?C Coupling of Allylic Alcohols with Free Indoles: Influence of the Metal Catalyst
Versatile reactive activities of allyl alcohols with free indoles in C?H functionalization reactions were investigated. Direct alkylation or cascade cyclization reactions could be selectively controlled based on the catalyst system: Ru(PPh3)3Cl2 provided C3-substituted beta-ketone indoles whereas [Ru(p-cymene)Cl2]2 yielded cyclized indoles.
A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 18514-76-6
Reference：
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N922 | ChemSpider