Reference of 87219-29-2, 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.87219-29-2, Name is (S)-Benzyl (5-oxotetrahydrofuran-3-yl)carbamate, molecular formula is C12H13NO4. In a article，once mentioned of 87219-29-2
The enantiospecific synthesis of functionalised pipecolic acids as constrained analogues of lysine
Two constrained analogues of (S)-lysine have been prepared, suitably protected for solid phase peptide synthesis, in high potential optical and diastereomeric purity. The key step is the alkylation of the 6-oxopipecolate derivative (6) with iodoacetonitrile.
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 87219-29-2
Reference：
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem