With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.4020-99-9,Methoxydiphenylphosphine,as a common compound, the synthetic route is as follows.
General procedure: Using the same stoichiometric ratio than in the previous reactions, the hexane solution was stirred at room temperature for 5 days. Then 5 mL of ethanol were added and the solution stirred for another 5 days. The solvent was then evaporated under vacuum and the residue purifiedby TLC. Compound 8d was obtained in 63% yield.
4020-99-9, As the paragraph descriping shows that 4020-99-9 is playing an increasingly important role.
Reference£º
Article; Gonzalez-Lopez, Vianney; Torres-Sandoval, Indira; Carrasco-Gonzalez, Ana L.; Elias-Jimenez, Adonay; Leyva, Marco A.; Rosales-Hoz, Maria J.; Cruz-Borbolla, Julian; Zuno-Cruz, Francisco J.; Sanchez-Cabrera, Gloria; Jardinez, Christian; Inorganica Chimica Acta; vol. 492; (2019); p. 8 – 17;,
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