111239-47-5Relevant articles and documents
Asymmetric Synthesis Catalyzed by Chiral Ferrocenylphosphine-Transition-Metal Complexes. 5. Palladium-Catalyzed Asymmetric Allylation of Active Methine Compounds
Hayashi, Tamio,Kanehira, Koichi,Hagihara, Toshiya,Kumada, Makoto
, p. 113 - 120 (1988)
Catalytic asymmetric allylation of sodium enolates of β-diketones with allyl acetate proceeded with high enantioselectivity in the presence of 0.5-1.0 mol percent of palladium complexes as catalysts bearing functionalized chiral ferrocenylphosphine ligand
Chiral phosphine ligands modified by crown ethers: An application to palladium-catalyzed asymmetric allylation of β-diketones
Sawamura, Masaya,Nagata, Hiroshi,Sakamoto, Hiroaki,Ito, Yoshihiko
, p. 2586 - 2592 (2007/10/02)
Chiral ferrocenylphosphine ligands modified by monoaza or diaza crown ethers of varying ring sizes and linker chain lengths (8a-e, 9) were synthesized. The reaction of the phosphine ligand modified by monoaza-18-crown-6 (8b) and the di-μ-chlorobis(T-allyl