Explore: Hydroformylation

In organic chemistry, hydroformylation, also known as oxo synthesis or oxo process, is an industrial process for the production of aldehydes (R−CH=O) from

Carbonylations are the basis of many types of reactions, including hydroformylation and Reppe reactions. These reactions require metal catalysts, which

known organocobalt chemistry. It is the parent member of a family of hydroformylation catalysts. Each molecule consists of two cobalt atoms bound to eight

particularly wide bite angle (108°). Such ligands are useful in the hydroformylation of alkenes. Illustrative of its wide bite angle, it forms both cis

hydrogen coproduct, but in modern times is not economically viable. The hydroformylation of methanol with catalysts like cobalt, nickel, or iron salts also

enantioselectivity in the hydroformylation of butenes and styrene. DIOP was the first chiral ligand used in the platinum-tin-catalyzed hydroformylation. The reactivity

methods for preparing aldehydes, one dominant technology is hydroformylation. Hydroformylation is conducted on a very large scale for diverse aldehydes.

is a yellow, benzene-soluble solid, which is used industrially for hydroformylation. [RhH(CO)(PPh3)3] was first prepared by the reduction of [RhCl(CO)(PPh3)2]

such as acetaldehyde in the traditional hydroacylation procedures. Hydroformylation is a classical transition-metal catalyzed reaction, and it has been

Diphosphines of wide bite angles are used in some industrial processes. The hydroformylation of alkenes to give aldehydes is an important industrial process. Almost