With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.24171-89-9,Tri(thiophen-2-yl)phosphine,as a common compound, the synthetic route is as follows.
Analogous to the reaction described above, Ru3(CO)12 (100 mg, 0.156 mmol) and PTh3 (44 mg, 0.157 mmol) in THF (20 mL) were treated with a few drops of Na[Ph2CO] in THF and the solution was stirred at 25 C for 30 min. Workup and chromatographic separation as described above afforded 1 (58 mg, 42%), 2 (15 mg, 8%), and 3 (7 mg, 3%)., 24171-89-9
As the paragraph descriping shows that 24171-89-9 is playing an increasingly important role.
Reference£º
Article; Uddin, Md Miaz; Begum, Noorjahan; Ghosh, Shishir; Sarker, Jagodish C.; Tocher, Derek A.; Hogarth, Graeme; Richmond, Michael G.; Nordlander, Ebbe; Kabir, Shariff E.; Journal of Organometallic Chemistry; vol. 812; (2016); p. 197 – 206;,
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