Some scientific research about 1273-94-5

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.SDS of cas: 1273-94-5, you can also check out more blogs about1273-94-5

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments. SDS of cas: 1273-94-5. Introducing a new discovery about 1273-94-5, Name is 1,1′-Diacetylferrocene

Formation of functionalized [3]ferrocenophane derivatives by an enamine condensation reaction

Treatment of 1,1?-diacetylferrocene (10) with excess piperidine and a stoichiometric amount of TiCl4 in pentane leads to CC-coupling of the two functional groups at the ferrocene framework. This enamine condensation reaction leads to the formation of the 1,3-connected dienamine-bridged [3]ferrocenophane system 13a. Complex 13a was characterised by X-ray crystal structure analysis. The analogous TiCl4-mediated coupling and condensation reactions of 10 with morpholine, pyrrolidine or methyl-isopropylamine yield the corresponding substituted [3]ferrocenophane systems 13b-d.

Formation of functionalized [3]ferrocenophane derivatives by an enamine condensation reaction

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.SDS of cas: 1273-94-5, you can also check out more blogs about1273-94-5

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