857722-03-3Relevant articles and documents
Modular multidentate phosphine ligands: Application to palladium-catalyzed allylic alkylations
Pei, Yuxin,Brule, Emilie,Moberg, Christina
, p. 544 - 550 (2006)
Multidentate phosphines were readily obtained by reaction of chiral multidentate amines, prepared via ring opening of (S)-N-tosyl-2- isopropylaziridine with ammonia, primary, and secondary amines, with achiral phosphorus containing building blocks. The phosphines were used in palladium-catalyzed alkylation of rac-3-cyclohexenyl and cyclopentenyl carbonates. The enantioselectivity and reactivity were largely dependent on the structure of the amine core of the ligands. Up to 88% ee was observed in reactions with the six-membered substrate. The Royal Society of Chemistry 2006.
Chelating phosphines with C2 and C3 symmetry
Brulé, Emilie,Pei, Yuxin,Lake, Fredrik,Rahm, Fredrik,Moberg, Christina
, p. 276 - 277 (2007/10/03)
Amide formation between ring opened aziridines and 2-(diphenylphosphino) benzoic acid provides an easy access to chelating di- and triphosphines with C2 and C3 symmetry.