Irreversible inhibitors are therefore the equivalent of poisons in heterogeneous catalysis. Application In Synthesis of 1,1′-Ferrocenedicarboxaldehyde, Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction by binding to a specific portion of an enzyme and thus slowing or preventing a reaction from occurring. In a patent£¬Which mentioned a new discovery about 1271-48-3
Synthesis and physico-analytical studies of some novel ferrocenyl Schiff base derivatives
A series of ferrocenyl Schiff base derivatives was synthesized by condensation reactions of 1,1?-ferrocenedicarboxaldehyde and aromatic amines containing long chain alkyl groups as free ends which were characterized by their physical properties, elemental, FTIR, 1H NMR, 13C NMR spectral and thermal analysis. The thermal behaviour of the synthesized compounds was studied by differential scanning calorimetry (DSC) which revealed that these compounds may exhibit mesomorphic properties. The DSC results of aromatic amines and ferrocenyl Schiff bases were compared to study the effects of structure, i.e. rigid core and terminal chain length, on the phase transition behaviour.
Synthesis and physico-analytical studies of some novel ferrocenyl Schiff base derivatives
If you are interested in 1271-48-3, you can contact me at any time and look forward to more communication. The potential utility of systematic synthetic strategy will be applicable to efficient generations of chemical libraries of compounds to find ¡®hit¡¯ molecules. Application In Synthesis of 1,1′-Ferrocenedicarboxaldehyde
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