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Selectivity in Palladium-Catalyzed Allylic Substitution | SpringerLink
Asymmetric allylic substitution by chiral palladium catalysts: Which is more reactive, major π-allyl Pd(II) species or minor π-allyl species? - ScienceDirect
Palladium-catalyzed tetraallylation of C60 with allyl chloride and allylstannane: Mechanism, regioselectivity, and enantioselectivity | Itami Organic Chemistry Laboratory, Nagoya University
Determination of Absolute Configuration of (π‐Allyl)Palladium Complexes by NMR Spectroscopy and Stereoselective Complexation - Gogoll - 2001 - Chemistry – A European Journal - Wiley Online Library
Synthesis and characterization of (π-allyl)palladium(II) complexes containing dialkylbiaryl phosphine ligands - ScienceDirect
Palladium Enolate Umpolung: Cyclative Diacetoxylation of Alkynyl Cyclohexadienones Promoted by a Pd/SPRIX Catalyst - Takenaka - 2014 - Angewandte Chemie International Edition - Wiley Online Library
Stereochemistry of the palladium-catalyzed allylic substitution: the syn-anti dichotomy in the formation of (π-allyl)palladium complexes and their equilibration - ScienceDirect
π-Allyl)palladium Complexes Bearing Diphosphinidenecyclobutene Ligands (DPCB): Highly Active Catalysts for Direct Conversion of Allylic Alcohols | Journal of the American Chemical Society
Synthesis, characterization, and reactivity of (π-allyl)palladium(II) wrap-around complexes with 1,3-dienes - ScienceDirect
Palladium-Catalyzed Asymmetric Allylic Alkylation/α-Iminol Rearrangement: A Facile Access to 2-Spirocyclic-Indoline Derivatives | CCS Chemistry
Effects of solvents, additives, and π-allyl ligand structures on the polymerization behavior of diazoacetates initiated by π-allylPd complexes - Polymer Chemistry (RSC Publishing)
π-Allyl)palladium Complexes Bearing Diphosphinidenecyclobutene Ligands (DPCB): Highly Active Catalysts for Direct Conversion of Allylic Alcohols | Journal of the American Chemical Society
Tsuji–Trost reaction - Wikipedia
Ligand-controlled regiodivergent π-allyl palladium catalysis enables a switch between [3+2] and [3+3] cycloadditions - Chemical Communications (RSC Publishing)