Reference of 1679-47-6, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.1679-47-6, Name is 3-Methyldihydrofuran-2(3H)-one, molecular formula is C5H8O2. In a Article，once mentioned of 1679-47-6
The kinetically controlled iodoetherification reaction of ethyl (S,E)-4,6-dihydroxy-2-hexenoate (1) gives the synthetically useful synthon 2, in which two new stereogenic centers have been generated, with selectivities up to 11:1.The mechanism of this allylic asymmetry transfer was probed by changing the allylic stereogenic substitutent, and the order of efficacy for asymmetric induction was found to be F>OH>/=OMe>Me.This result ruled out several proposed mechanisms of asymmetry transfer and led to the proposal of a transition-structure model, based on AM1 calculations.Our model rationalizes all of our results as well as those from the literature concerning selectivity and even relative rates of diastereomeric substrates.
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 1679-47-6
Reference：
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem