Brief introduction of Ethyl 2-oxotetrahydrofuran-3-carboxylate

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.Computed Properties of C7H10O4, you can also check out more blogs about77513-58-7

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments. Computed Properties of C7H10O4. Introducing a new discovery about 77513-58-7, Name is Ethyl 2-oxotetrahydrofuran-3-carboxylate

Substrate-directable reactions play a pivotal role in organic synthesis, but are uncommon in reactions proceeding via radical mechanisms. Herein, we provide experimental evidence showing dramatic rate acceleration in the Sm(II)-mediated reduction of cyclic esters that is enabled by transient chelation between a directing group and the lanthanide center. This process allows unprecedented chemoselectivity in the reduction of cyclic esters using SmI2-H2O and for the first time proceeds with a broad substrate scope. Initial studies on the origin of selectivity and synthetic application to form carbon-carbon bonds are also disclosed.

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.Computed Properties of C7H10O4, you can also check out more blogs about77513-58-7

Reference：
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem