Improvement of chiral stationary phases based on cinchona alkaloids bonded to crown ethers by chiral modification was written by Zhao, Jianchao;Wu, Haixia;Wang, Dongqiang;Wu, Haibo;Cheng, Lingping;Jin, Yu;Ke, Yanxiong;Liang, Xinmiao. And the article was included in Journal of Separation Science in 2015.Related Products of 297752-25-1 This article mentions the following:
To improve the chiral recognition capability of a cinchona alkaloid crown ether chiral stationary phase, the crown ether moiety was modified by the chiral group of (1S,2S)-2-aminocyclohexyl phenylcarbamate. Both quinine and quinidine-based stationary phases were evaluated by chiral acids, chiral primary amines and amino acids. The quinine/quinidine and crown ether provided ion-exchange sites and complex interaction site for carboxyl group and primary amine group in amino acids, resp., which were necessary for the chiral discrimination of amino acid enantiomers. The introduction of the chiral group greatly improved the chiral recognition for chiral primary amines. The structure of crown ether moiety was proved to play a dominant role in the chiral recognitions for chiral primary amines and amino acids. In the experiment, the researchers used many compounds, for example, (R)-4-Hydroxy-8,9,10,11,12,13,14,15-octahydrodinaphtho[2,1-d:1′,2′-f][1,3,2]dioxaphosphepine 4-oxide (cas: 297752-25-1Related Products of 297752-25-1).
(R)-4-Hydroxy-8,9,10,11,12,13,14,15-octahydrodinaphtho[2,1-d:1′,2′-f][1,3,2]dioxaphosphepine 4-oxide (cas: 297752-25-1) belongs to chiral phosphine ligands. Phosphine-catalyzed asymmetric reactions are now powerful and versatile tools for the construction of C–C, C–N, C–O, and C–S bonds and for the syntheses of functionalized carbocycles and heterocycles. Trivalent phosphorus compounds called phosphines have a tetrahedral electron-group geometry which makes them structurally analogous to amines.Related Products of 297752-25-1
Referemce:
Phosphine ligand,
Chiral phosphines in nucleophilic organocatalysis