Synthetic Route of 1271-48-3, Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. 1271-48-3, Name is 1,1′-Ferrocenedicarboxaldehyde, molecular weight is 242.0516. In an Article，once mentioned of 1271-48-3
Condensation of carotinoid polyene dialdehydes, 1,1?-ferrocene dialdehydes and of 9-ferrocenyl-2,7-dimethylnonatetraenal with the Fischer carbene complexes (OC)5W=C(NM2)CH2SiMe3 or (OC)5M=C(Me)(OMe) (M=Cr, W) in the presence of n-BuLi or SiM3Cl/NEt3 yields the bis(carbene) complexes 1-4 and the donor acceptor substituted complexes 5, 6. The star-shaped trinuclear molecules 7 and 8 were obtained under Wittig conditions from 1,3,5-tris[(triphenylphosphonio)methyl]benzene tribromide and ferrocene aldehyde or 9-ferrocenyl-2,7-dimethyl-nonatetraenal.
Hydrocarbon bridged metal complexes XLV. Dinuclear polyene-bridged Fischer carbene complexes and a star-shaped benzene-bridged tris(ferrocenyl-decapentaenyl) compound
Therefore, this conceptually novel strategy might open impressive avenues to establish green and sustainable chemistry platforms. In my other articles, you can also check out more blogs about 1271-48-3
Reference：
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