P-Chiral phosphine

P-Chiral phosphines are organophosphorus compounds of the formula PRR′R″, where R, R′, R″ = H, alkyl, aryl, etc. They are a subset of chiral phosphines, a broader class of compounds where the stereogenic center can reside at sites other than phosphorus. P-chirality exploits the high barrier for inversion of phosphines, which ensures that enantiomers of PRR'R" do not racemize readily. The inversion barrier is relatively insensitive to substituents for triorganophosphines.[2] By contrast, most amines of the type NRR′R″ undergo rapid pyramidal inversion.

Two P-chiral "Kwon phosphines".[1]

Research themes

Most chiral phosphines are C2-symmetric diphosphines. Famous examples are DIPAMP and BINAP. These chelating ligands support catalysts used in asymmetric hydrogenation and related reactions. DIPAMP is prepared by coupling the P-chiral methylphenylanisylphosphine.

P-Chiral phosphines are of particular interest in asymmetric catalysis. P-Chiral phosphines have been investigated for two main applications, as ligands for asymmetric homogeneous catalysts and as nucleophiles in organocatalysis.[1]

gollark: Congratulatory apioids, generally.
gollark: That happened to me this morning. It was very unpleasant.
gollark: Sounds efficient!
gollark: If you emulate CC in BeeVM, certainly.
gollark: https://git.osmarks.net/osmarks/potatOS/

References
  1. Xiao, Y.; Sun, Z.; Guo, H.; Kwon, O. (2014). "Chiral Phosphines in Nucleophilic Organocatalysis". Beilstein Journal of Organic Chemistry. 10: 2089–2121. doi:10.3762/bjoc.10.218. PMC 4168899.CS1 maint: uses authors parameter (link)
  2. Mislow, Kurt; Baechler, Raymond D. (1971). "Effect of ligand electronegativity on the inversion barrier of phosphines". Journal of the American Chemical Society. 93 (3): 773–774. doi:10.1021/ja00732a036.
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