Reference of 32005-36-0, 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.32005-36-0, Name is Bis(dibenzylideneacetone)palladium, molecular formula is C34H28O2Pd. In a article，once mentioned of 32005-36-0
A solely planar chiral pseudo-C2-symmetric ferrocene-based P,S-chelating 2 was prepared and applied to some asymmetric reactions. Although a poor enantioselectivity is obtained in the asymmetric allylic alkylation (AAA) of rac-8 using the Pd complex bearing the P,S-hybrid ligand 2, it is noteworthy that this result is superior to that obtained using the C2-symmetric bisphosphine counterpart of 2. The intermolecular asymmetric heck reaction (AHR) of 11 with aryl triflates catalyzed by another palladium complex containing 2 was also carried out. Although both relatively low reactivity and poor enantioselectivity were obtained, a high regioselectivy favoring the 2,5-dihydrofuran derivative (14) over the regioisomeric 2,3-dihydrofuran derivative (15) was observed in this study.
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 32005-36-0
Reference：
Chapter 1 An introduction to palladium catalysis,
Palladium/carbon catalyst regeneration and mechanical application method