(R,R)-N,N′-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminoaluminium(III) chloride (CAS 250611-13-3)

(R,R)-N,N′-Bis(3,5-Di-Tert-Butylsalicylidene)-1,2-Cyclohexanediaminoaluminium(Iii) Chloride functions as a catalyst in various organic transformations, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. Its mechanism of action involves the activation of substrates through coordination to the aluminum center, followed by the transfer of the ligand to the substrate, leading to the desired chemical transformation. The chelating ligand framework provides a rigid environment for the aluminum center, enhancing its reactivity and selectivity in catalytic processes. (R,R)-N,N′-Bis(3,5-Di-Tert-Butylsalicylidene)-1,2-Cyclohexanediaminoaluminium(Iii) Chloride′s ability to facilitate asymmetric transformations may be in the synthesis of chiral molecules. Its coordination to the aluminum center allows for the stabilization of reactive intermediates, enabling the execution of challenging transformations with high efficiency. (R,R)-N,N′-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminoaluminium(III) chloride plays a significant role in promoting various organic reactions by facilitating the activation of substrates and controlling the stereochemistry of the resulting products.