Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. 6372-42-5, Name is Cyclohexyldiphenylphosphine, molecular formula is C18H21P, belongs to chiral-phosphine-ligands compound. In a document, author is Dan, Hu-Guang, introduce the new discover, Category: chiral-phosphine-ligands.
Recent Advances in Amino Acid-Based Phosphine Catalysts and Their Applications in Asymmetric Reactions
Amino acid-based catalysts have been intensively researched in recent years. Amino acid-derived phosphines possess high nucleophilicity and exhibit unique catalytic activities in asymmetric synthesis. L-Threonine and valine are most utilized natural amino acids in the preparation of chiral phosphines. The efficient and versatile chiral phosphine catalysts are applied in a wide range of reactions such as MBH reaction, Rauhut-Currier reaction, Michael addition, [4 + 2]-annulation, [3 + 2]-annulation, 1,4-dipolar cycloaddition. They are also widely used in the construction of core structures of natural products. Amino acid-based phosphine catalysts and their applications in asymmetric synthesis are summarized.
Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law. In my other articles, you can also check out more blogs about 6372-42-5. Category: chiral-phosphine-ligands.
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