More research is needed about 1,1′-Diacetylferrocene

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Application of 1273-94-5. In my other articles, you can also check out more blogs about 1273-94-5

Application of 1273-94-5, Chemistry is the science of change. But why do chemical reactions take place? Why do chemicals react with each other? The answer is in thermodynamics and kinetics.In a document type is Article, and a compound is mentioned, 1273-94-5, 1,1′-Diacetylferrocene, introducing its new discovery.

Stereo- and enantioselectivity in catalytic hydrogenolysis of chiral substituted ferrocenes to give cyclopentanes

The catalytic hydrogenolysis of 1,2-disubstituted ferrocenes having planar chirality and functional groups such as carboxyl (including ester) or tertiary amino proceeds under mild conditions (1 atm of H2, Pd/C, CF3COOH, 50 deg C) with the retention of functional groups in the cyclopentane products.Stereosectivity has been observed for the examples investigated, the diastereomeric ratio, trans: cis being close to 4:1, but optically inactive products are formed the enantiomeric ferrocenes.In contrast, hydrogenolysis of enantiomeric alpha-(N,N-dimethylamino)ethylferrocene gives an optically active alpha-(N,N-dimethylamino)ethylcyclopentane with retention of configuration at the alpha-carbon, whose bonds are not affected during the hydrogenolysis.

Stereo- and enantioselectivity in catalytic hydrogenolysis of chiral substituted ferrocenes to give cyclopentanes

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Application of 1273-94-5. In my other articles, you can also check out more blogs about 1273-94-5

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