Final Thoughts on Chemistry for Di(adamantan-1-yl)phosphine

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. 131211-27-3, In my other articles, you can also check out more blogs about 131211-27-3

131211-27-3. Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 131211-27-3, Name is Di(adamantan-1-yl)phosphine

General synthesis and catalytic applications of di(1-adamantyl) alkylphosphines and their phosphonium salts

An improved synthesis of di(1-adamantyl)alkylphosphines by alkylation of di(1-adamantyl)phosphine followed by deprotonation of the resulting phosphonium halide is described. Compared to previous protocols for the synthesis of this class of compounds, the procedure does not require chlorination of the secondary phosphine by phosgene, or formation of sensitive lithium di(1-adamantyl) phosphide. Selected examples of the prepared phosphonium salts and phosphines are shown to be excellent ligands for the palladium-catalyzed cross-coupling reaction of chloroarenes with arylboronic acids.

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. 131211-27-3, In my other articles, you can also check out more blogs about 131211-27-3

Reference£º
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