Analyzing the synthesis route of 1663-45-2

After consulting a lot of data, we found that this compound(1663-45-2)Name: 1,2-Bis(diphenylphosphino)ethane can be used in many types of reactions. And in most cases, this compound has more advantages.

Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Journal, ACS Catalysis called Synthesis of Phosphinines from CoII-Catalyzed [2+2+2] Cycloaddition Reactions, Author is Glaesel, Tim; Jiao, Haijun; Hapke, Marko, which mentions a compound: 1663-45-2, SMILESS is P(CCP(C1=CC=CC=C1)C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4, Molecular C26H24P2, Name: 1,2-Bis(diphenylphosphino)ethane.

The CoII-catalyzed [2+2+2] cycloaddition of functionalized diynes and phosphaalkynes resulting in the formation of an array of structurally interesting phosphinines is reported. A combination of 1,2-bis(diphenylphosphino)benzene (dppbenz) and CoI2 turned out to be the most suitable and active catalyst system under microwave reaction conditions. Chemoselective cyclizations of phosphaalkynes in the presence of nitriles have been observed, and a number of carbonyl functionalities are tolerated as well. The reaction can successfully be conducted with a 1:1 ratio of phosphaalkyne/diyne substrate. Model reactions with benzonitrile and diyne demonstrated that CoII catalysts in the presence of bisphosphines prefer carbocyclization, while reduction to lower oxidation states promotes heterocyclization to the corresponding pyridine. A reaction mechanism comprising a CoII oxidation state for the cyclotrimerization process is proposed and rationalized based on control experiments and theor. calculations

After consulting a lot of data, we found that this compound(1663-45-2)Name: 1,2-Bis(diphenylphosphino)ethane can be used in many types of reactions. And in most cases, this compound has more advantages.

Reference:
Chiral nitrogen ligands in late transition metal-catalysed asymmetric synthesis—I. Addressing the problem of ligand lability in rhodium-catalysed hydrosilations,
Nitrogen-Containing Ligands for Asymmetric Homogeneous and Heterogeneous Catalysis