Reference of 288-14-2, 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.288-14-2, Name is Isoxazole, molecular formula is C3H3NO. In a article，once mentioned of 288-14-2
Recent Advances in Green Synthesis of 3,3?-Spirooxindoles via Isatin?based One?pot Multicomponent Cascade Reactions in Aqueous Medium
3,3?-spirooxindoles are important synthetic target compounds and play special role in organic chemistry because of their extensive biological activities and applications of pharmaceutical lead discovery. In recent years, there has been a significant increase in design of new, atom economical and eco-friendly isatin-based one-pot multicomponent cascade reactions in aqueous medium for the green synthesis of 3,3?-spirooxindoles. In this review, the recent advances in this area were summarized and classified according to catalyst-free, organic-catalyzed, inorganic-catalyzed, nanometer-silica-catalyzed and enzyme-catalyzed reaction systems. These reviewed methods provide important inspiration for the synthesis of novel 3,3?-spirooxindoles and design of new pharmaceutical compounds.
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 288-14-2
Reference：
Isoxazole – Wikipedia,
Isoxazole | C3H3NO – PubChem