4265-16-1, 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.4265-16-1, Name is Benzo[b]furan-2-carboxaldehyde, molecular formula is C9H6O2. In a article£¬once mentioned of 4265-16-1
A Unified Strategy for the Synthesis of beta-Carbolines, gamma-Carbolines, and Other Fused Azaheteroaromatics under Mild, Metal-Free Conditions
An efficient, unified approach for the synthesis of beta-carbolines, gamma-carbolines, and other fused azaheteroaromatics has been realized under metal-free conditions, from propargylic amines and (hetero)aromatic aldehydes. This unified strategy provides beta- and gamma-carbolines as well as a range of fused azaheteroaromatics with a broad substrate scope and excellent functional group compatibility. The formal synthesis of oxopropalines D and G has been achieved on gram scale (3a), in a one-pot reaction from commercially available materials (previous shortest reported route to 3a was 5 steps). NMR studies of the conversion of imine intermediate 3aa to beta-carboline 3a were conducted and revealed that the reaction proceeded through an allene intermediate.
A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. 4265-16-1, In my other articles, you can also check out more blogs about 4265-16-1
Reference£º
Benzofuran – Wikipedia,
Benzofuran | C8H1081O – PubChem