Application of 4265-16-1, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 4265-16-1, Name is Benzo[b]furan-2-carboxaldehyde, molecular formula is C9H6O2. In a Article，once mentioned of 4265-16-1
In contrast to the catalytic asymmetric dearomative reactions of indole substrates, those of the analogous benzofuran derivatives have been less explored. Here we report that the stereoselective domino Rauhut-Currier/Michael addition process of 3-benzofuranyl vinyl ketones and 3-olefinic (7-aza)oxindoles can be realised via catalysis by a chiral bifunctional phosphine, furnishing the previously unreported direct asymmetric dearomative reaction of benzofuran substrates tethered to a carbonyl group in a formal [4+2] cycloaddition manner. An array of hydrodibenzofuran derivatives with dense substitutions is generally constructed with excellent diastereoselectivity and enantioselectivity (up to >191 dr, >99% ee).
Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Application of 4265-16-1. In my other articles, you can also check out more blogs about 4265-16-1
Reference：
Benzofuran – Wikipedia,
Benzofuran | C8H1110O – PubChem