Synthetic Route of 1273-86-5, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.1273-86-5, Name is Ferrocenemethanol, molecular formula is C11H3FeO. In a Article£¬once mentioned of 1273-86-5
Synthesis and enantiomeric resolution of ferrocenyl(alkyl)azoles
Ferrocenyl(alkyl)azoles were synthesized in high yields by interaction of alpha-ferrocenylcarbinoles with azoles in aqueous-organic in the presence of HBF4 or by interaction of alpha-ferrocenylcarbinoles with N,N?-carbonyldiimidazole, N,N?-thionyldiimidazole, N,N?-thionyldibenzimidazole in boiling dichloromethane. The resulting enantiomers of ferrocenyl(alkyl) azoles and some carbinoles were separated using HPLC on silica bonded chiral stationary phases based on cyclodextrins and modified cellulose.
Synthesis and enantiomeric resolution of ferrocenyl(alkyl)azoles
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 1273-86-5
Reference£º
Iron Catalysis in Organic Synthesis | Chemical Reviews,
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion