With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.18437-78-0,Tris(4-fluorophenyl)phosphine,as a common compound, the synthetic route is as follows.
General procedure: Complex 1a (24 mg, 0.03 mmol) and appropriate triarylphosphine(0.06 mmol) were suspended in 5ml of acetone, andthe reaction mixture was ultrasonicated for 2 h. The resulting suspensionwas evaporate to dryness and the dry residue was chromatographedon Silica (eluent dichloromethane: methanol = 4: 1)to afford yellow-orange solid of 2a-d.
18437-78-0, As the paragraph descriping shows that 18437-78-0 is playing an increasingly important role.
Reference£º
Article; Zhukovsky, Daniil D.; Sizov, Vladimir V.; Starova, Galina L.; Tunik, Sergey P.; Grachova, Elena V.; Journal of Organometallic Chemistry; vol. 867; (2018); p. 367 – 374;,
Phosphine ligand
Chiral phosphine ligands in asymmetric synthesis. Molecular structure and absolute configuration of (1,5-cyclooctadiene)-(2S,3S)-2,3-bis(diphenylphosphino)butanerhodium(I) perchlorate tetrahydrofuran solvate