Brief introduction of 1,1′-Ferrocenedicarboxaldehyde

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.Product Details of 1271-48-3, you can also check out more blogs about1271-48-3

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments. Product Details of 1271-48-3. Introducing a new discovery about 1271-48-3, Name is 1,1′-Ferrocenedicarboxaldehyde

Syntheses of chiral ferrocenophanes and their application to asymmetric catalysis

N-Substituted 2-aza-[3]-ferrocenophanes were easily synthesized from 1,1?-ferrocenedicarbaldehyde and aliphatic amines in high yields. One of the ferrocenophanes served as a ligand for the copper-catalyzed oxidative coupling of 2-naphthol derivatives to give the products in good yields with up to 92% ee, and it also efficiently catalyzed the asymmetric Michael addition reaction as an organocatalyst.

Syntheses of chiral ferrocenophanes and their application to asymmetric catalysis

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.Product Details of 1271-48-3, you can also check out more blogs about1271-48-3

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