New explortion of 4-(4-Chlorophenyl)dihydro-2H-pyran-2,6(3H)-dione

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.Application In Synthesis of 4-(4-Chlorophenyl)dihydro-2H-pyran-2,6(3H)-dione, you can also check out more blogs about53911-68-5

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.53911-68-5, Name is 4-(4-Chlorophenyl)dihydro-2H-pyran-2,6(3H)-dione, molecular formula is C11H9ClO3. In a Article£¬once mentioned of 53911-68-5, Application In Synthesis of 4-(4-Chlorophenyl)dihydro-2H-pyran-2,6(3H)-dione

Studies on enzymatic synthesis of chiral non-racemic 3-arylglutaric acid monoesters

The enantioselective enzymatic desymmetrization (EED) of various 3-arylglutaric anhydrides 1 with alcohols in organic media has been studied. The effect of the solvent on the stereochemical outcome of the reaction was investigated in detail. The amount of biocatalyst was optimized, and the possibility of its re-use was tested. The first example of the EED of 3-substituted glutaric anhydrides with esters as nucleophiles is reported.

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.Application In Synthesis of 4-(4-Chlorophenyl)dihydro-2H-pyran-2,6(3H)-dione, you can also check out more blogs about53911-68-5

Reference£º
Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics