Related Products of 18959-30-3, 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.18959-30-3, Name is 4,5-Difluorophthalic Anhydride, molecular formula is C8H2F2O3. In a article，once mentioned of 18959-30-3
A formal [4+2] cycloaddition of alpha,alpha?-dichloro-ortho-xylenes with various alkynes has been developed using a low-valent cobalt catalyst. The transformation has a wide substrate scope and high functional-group tolerance and led to 1,4-dihydronaphthalenes. The formed cycloadducts were easily aromatized with MnO2 under air. A mechanistic investigation suggests that the transformation proceeds through a benzyl cobaltation of alkyne, not the classical Diels-Alder reaction of ortho-quinodimethanes. This methodology provides a straightforward and streamlined access to linearly expanded pi-conjugated aromatics. Simple, but powerful: The title reaction leads to 1,4-dihydronaphthalenes with a wide substrate scope and high functional-group tolerance. Mechanistic investigation supports a benzyl cobaltation of alkyne, not the classical Diels-Alder reaction of ortho-quinodimethanes. This methodology provides a straightforward access to linearly expanded pi-conjugated aromatics.
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 18959-30-3
Reference：
Benzofuran – Wikipedia,
Benzofuran | C8H2942O – PubChem