255904-80-4Relevant academic research and scientific papers
Reactivity of metallophosphide anions with electrophilic (arene)tricarbonylmetal complexes
Comte, Virginie,Tranchier, Jean Philippe,Rose-Munch, Francoise,Rose, Eric,Perrey, Daniele,Richard, Philippe,Moise, Claude
, p. 1893 - 1899 (2007/10/03)
Reaction of metallophosphide anions [(CO)xM′PPh2]- (M′ = Cr, Fe) with neutral tricarbonyl(η6-fluoroarene) chromium and cationic (η6-arene)tricarbonylmanganese complexes give rise to the formation of dinuclear co
The asymmetric synthesis of phosphorus- and sulfur-containing tricarbonyl(η6-arene)chromium complexes using the chiral base approach
Ariffin, Azhar,Blake, Alexander J.,Ewin, Richard A.,Li, Wan-Sheung,Simpkins, Nigel S.
, p. 3177 - 3189 (2007/10/03)
The use of a simple chiral lithium amide base 2 enables the asymmetric transformation of tricarbonyl-[η6-(diphenylphosphinoyl)benzene]chromium(0) 12 into the corresponding ortho-silylated complex in up to 86% ee. A tin derivative was prepared similarly and was then used to prepare other derivatives via reduction to the corresponding phosphine, followed by transmetallation-electrophilic quench. In the case of tricarbonyl-(η6-1,3-dihydroisobenzothiophene)chromium(0) the chiral base 2 was ineffective, and it was necessary to use a bis-lithium amide base 9 to effect asymmetric substitution in high ee (up to 95%). Decomplexation gave the corresponding chiral sulfides in highly enantiomerically enriched form. In all cases the absolute stereochemistry of the products was derived by conducting X-ray structure determinations on selected examples. The Royal Society of Chemistry 1999.
