Some scientific research about C18H21P

Reference of 6372-42-5, Each elementary reaction can be described in terms of its molecularity, the number of molecules that collide in that step. The slowest step in a reaction mechanism is the rate-determining step.you can also check out more blogs about 6372-42-5.

Reference of 6372-42-5, Children learn through play, and they learn more than adults might expect. Science experiments are a great way to spark their curiosity, 6372-42-5, Name is Cyclohexyldiphenylphosphine, SMILES is C1CCC(CC1)P(C1=CC=CC=C1)C1=CC=CC=C1, belongs to chiral-phosphine-ligands compound. In a article, author is Yanagisawa, Akira, introduce new discover of the category.

Asymmetric Allylation of Carbonyl Compounds Catalyzed by a Chiral Phosphine-Silver Complex

A catalytic, asymmetric allylation reaction of aldehydes or ketones with allyltrimethoxysilane was achieved by using a BINAPAgBF(4) [BINAP = 2,2-bis(diphenylphosphino)-1,1-binaphthyl] complex as the chiral precatalyst and triethylamine as the base precatalyst in the presence of 2,2,2-trifluoroethanol. Optically active homoallylic alcohols with up to 95%ee were obtained in moderate to high yields through the in situ generated chiral allyl silver catalyst.

Reference of 6372-42-5, Each elementary reaction can be described in terms of its molecularity, the number of molecules that collide in that step. The slowest step in a reaction mechanism is the rate-determining step.you can also check out more blogs about 6372-42-5.

Reference:
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