@article {9866,
	title = {Chiral Phosphaalkene-Oxazoline Ligands for the Palladium-Catalyzed Asymmetric Allylic Alkylation.},
	journal = {Organic Letters},
	volume = {12},
	year = {2010},
	note = {CAPLUS AN 2010:1194962(Journal)},
	month = {2010///},
	pages = {4667 - 4669},
	publisher = {American Chemical Society},
	abstract = {Enantioselective catalysis in moderate to excellent yields and ee{\textquoteright}s has been accomplished using a phosphaalkene-based ligand system. Specifically, the palladium-catalyzed allylic alkylation of 1,3-diphenyl-2-propenyl acetate using a chiral P(sp2),N(sp2) ligand proceeds with a variety of malonate nucleophiles to give the desired malonates, e.g. I, in 73-95\% yield (79-92\% ee). [on SciFinder(R)]},
	keywords = {diphenylallyl malonate prepn phosphaalkene oxazoline palladium catalyzed allylic alkylation, diphenylpropenyl acetate malonate reactant stereoselective allylic alkylation palladium catalyst, enantioselective palladium catalyzed allylic alkylation phosphaalkene oxazoline ligand},
	isbn = {1523-7060},
	author = {Dugal-Tessier,Julien and Dake, G. R. and Gates, Derek P}
}
