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Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Quality Control of Benzo[b]furan-2-carboxaldehyde, you can also check out more blogs about4265-16-1

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments. Quality Control of Benzo[b]furan-2-carboxaldehyde. Introducing a new discovery about 4265-16-1, Name is Benzo[b]furan-2-carboxaldehyde

(Chemical Equation Presented) We present an efficient synthesis of beta-hydroxyesters and R,beta-unsaturated esters via activation of the silicon-carbon bond of alpha-trimethylsilylethylacetate using catalytic amounts of the commercially available P(i-PrNCH2CH2) 3N 1a. Selectivity for either of these two products can be achieved simply by altering the catalyst loading and reaction temperature to afford addition or stereoselective condensation. This method is mild and tolerates a wide array of functional groups.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Quality Control of Benzo[b]furan-2-carboxaldehyde, you can also check out more blogs about4265-16-1

Reference：
Benzofuran – Wikipedia,
Benzofuran | C8H1091O – PubChem