Some tips on 29949-84-6

29949-84-6 Tris(3-methoxyphenyl)phosphine 141534, achiral-phosphine-ligands compound, is more and more widely used in various.

29949-84-6, Tris(3-methoxyphenyl)phosphine is a chiral-phosphine-ligands compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

A large amount of microcrystalline the preparation of the sample: weighing 0.3mmol of cuprous iodide is dissolved in 10 ml acetonitrile to obtain solution A, weighing 0.3mmol m – anisyl3 P ligand dissolved in 10 ml dichloromethane to obtain solution B, the solution A and solution B mixed, and stirring to make fully undergo coordination reaction, and finally the resulting colorless solution is filtered, and steaming and remove all solvent, vacuum drying, to obtain the colorless crystal powder is the product, yield 96% (to Cu meter)., 29949-84-6

29949-84-6 Tris(3-methoxyphenyl)phosphine 141534, achiral-phosphine-ligands compound, is more and more widely used in various.

Reference£º
Patent; China Jiliang University; Chai, Wenxiang; Tian, Yuan; Song, Li; Tao, Xiaoyong; Huang, Jiayan; Zhang, Ming; Chen, Haichao; Chen, Zhi; (10 pag.)CN104893715; (2017); B;,
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

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As the paragraph descriping shows that 29949-84-6 is playing an increasingly important role.

29949-84-6, Tris(3-methoxyphenyl)phosphine is a chiral-phosphine-ligands compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

General procedure: Under a N2 atmosphere, phosphine ligand (2 mmol) (L) was added to a stirred solution of Co2(CO)8 (1 mmol) in tetrahydrofuran or toluene (10 mL). The reaction mixture was stirred for 1 h under CO bubbling at 50 C. The organic solvent was evaporated under reduced pressure. The resulting solid was washed several times with diethyl ether and pentane, finally dried under vacuum to give the desired complex.

As the paragraph descriping shows that 29949-84-6 is playing an increasingly important role.

Reference£º
Article; Amezquita-Valencia, Manuel; Ramirez-Garavito, Ricardo; Toscano, Ruben A.; Cabrera; Catalysis Communications; vol. 33; (2013); p. 29 – 33;,
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