Zheng, Yin; Qin, Tianzhu; Zi, Weiwei published an article in 2021. The article was titled 《Enantioselective Inverse Electron Demand (3 + 2) Cycloaddition of Palladium-Oxyallyl Enabled by a Hydrogen-Bond-Donating Ligand》, and you may find the article in Journal of the American Chemical Society.SDS of cas: 51364-51-3 The information in the text is summarized as follows:
A method for enantioselective (3 + 2) cycloaddition reactions between palladium-oxyallyl species and electron-deficient nitroalkenes has been reported. This transformation is enabled by a rationally designed hydrogen-bond-donating ligand (FeUrPhos) and proceeds via an inverse electron demand pathway. Using this method, cyclopentanones I (R = n-Bu, Ph, PhCH2CH2, 4-MeC6H4, 3-ClC6H4, 2-naphthyl, etc.; R1 = H, R2 = H, 2-O2NC6H4, 4-FC6H4, 2-naphthyl, etc; R1 = Me, R2 = H) with up to three contiguous stereocenters were assembled with high enantioselectivity and good to excellent diastereoselectivity from cyclic carbonates II and nitroalkenes O2NCR1:CHR2. In the experimental materials used by the author, we found Tris(dibenzylideneacetone)dipalladium(0)(cas: 51364-51-3SDS of cas: 51364-51-3)
Tris(dibenzylideneacetone)dipalladium(0)(cas: 51364-51-3) is the most widely used PdO precursor complex in synthesis and catalysis, in particular as a catalyst for various coupling reactions. SDS of cas: 51364-51-3 It is used as a catalyst precursor for palladium-catalyzed carbon-nitrogen bond formation, conversion of aryl chlorides, triflates and nonaflates to nitroaromatics.
Referemce:
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI