Reactions catalyzed interfaces commonly occur at high coverage and in condensed media, causing turnover rates to depend on composition, collectively referred to as solvent effects. In a patent，Which mentioned a new discovery about 2879-20-1, 2879-20-1
Pyrrolo[1,2-a]quinoxalines were synthesized through a three-component reaction of 2-alkoxy-2,3-dihydrofuran, o-phenylenediamine and ketone. This reaction was performed in nitromethane by using boron trifluoride etherate as catalyst. Mechanism of this reaction involves the following two steps: (i) a condensation reaction of the dihydrofuran with o-phenylenediamine, which produced a N-(2-aminophenyl)pyrrole derivative that can act as a 1,5-bisnucleophile, and (ii) an intramolecular Mannich-type reaction of the bisnucleophile and ketone to produce the pyrrolo[1,2-a]quinoxaline derivative.
A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. 2879-20-1, In my other articles, you can also check out more blogs about 2879-20-1