Palladium‐Catalyzed Electrophilic Allylation Reactions via Bis(allyl) palladium Complexes and Related Intermediates - Szabó - 2004 - Chemistry – A European Journal - Wiley Online Library
Scheme 3. Part of the mechanism for the palladium catalyzed allylic... | Download Scientific Diagram
Relative Rates for the Amination of η3-Allyl and η3-Benzyl Complexes of Palladium | Journal of the American Chemical Society
Mechanistic Investigations of Palladium-Catalyzed Allylic Fluorination | Organometallics
Air-Stable Pd(R-allyl)LCl (L= Q-Phos, P(t-Bu)3, etc.) Systems for C–C/N Couplings: Insight into the Structure–Activity Relationship and Catalyst Activation Pathway | The Journal of Organic Chemistry
Synergistic Organoboron/Palladium Catalysis for Regioselective N-Allylations of Azoles with Allylic Alcohols | Organic Letters
Formation of Palladium(0) Complexes from Pd(OAc)2 and a Bidentate Phosphine Ligand (dppp) and Their Reactivity in Oxidative Addition | Organometallics
Palladium -catalyzed tetraallylation of C 60 with allyl chloride and allylstannane : mechanism, regioselectivity, and enantioselectivity - Chemical Science (RSC Publishing) DOI:10.1039/C2SC21126B
Catalytic allylic functionalization via π-allyl palladium chemistry - Organic & Biomolecular Chemistry (RSC Publishing)
![Comparative reactivity of allylic alcohols. Conditions: [Pd] ) 0.0055 M... | Download Scientific Diagram](https://www.researchgate.net/publication/244460612/figure/fig1/AS:298491034259456@1448177216307/Comparative-reactivity-of-allylic-alcohols-Conditions-Pd-00055-M-in-water-at-25.png "Comparative reactivity of allylic alcohols. Conditions: [Pd] ) 0.0055 M... | Download Scientific Diagram")
Comparative reactivity of allylic alcohols. Conditions: [Pd] ) 0.0055 M... | Download Scientific Diagram
![Allyl–palladium complexes with fluorinated benzene thiolate ligands. Examination of the electronic effects in the Pd-catalyzed allylic alkylation reaction with the catalytic system [(η3-C3H5)Pd(μ-SRf)]2/PR3 - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0022328X02012251-loc1.gif "Allyl–palladium complexes with fluorinated benzene thiolate ligands. Examination of the electronic effects in the Pd-catalyzed allylic alkylation reaction with the catalytic system [(η3-C3H5)Pd(μ-SRf)]2/PR3 - ScienceDirect")
Allyl–palladium complexes with fluorinated benzene thiolate ligands. Examination of the electronic effects in the Pd-catalyzed allylic alkylation reaction with the catalytic system [(η3-C3H5)Pd(μ-SRf)]2/PR3 - ScienceDirect
Molecules | Free Full-Text | Palladium and Organocatalysis: An Excellent Recipe for Asymmetric Synthesis
Palladium‐Catalyzed Electrophilic Allylation Reactions via Bis(allyl) palladium Complexes and Related Intermediates - Szabó - 2004 - Chemistry – A European Journal - Wiley Online Library
Palladium‐Catalyzed Allyl Cross‐Coupling Reactions with In Situ Generated Organoindium Reagents - Lee - 2011 - Chemistry – An Asian Journal - Wiley Online Library
Palladium-Catalyzed Allylic Alkylation via Photocatalytic Nucleophile Generation | ACS Catalysis
Palladium‐Catalyzed Allyl Cross‐Coupling Reactions with In Situ Generated Organoindium Reagents - Lee - 2011 - Chemistry – An Asian Journal - Wiley Online Library
Palladium‐Catalyzed Electrophilic Allylation Reactions via Bis(allyl) palladium Complexes and Related Intermediates - Szabó - 2004 - Chemistry – A European Journal - Wiley Online Library
Allylic Amination of Pd(II)-Allyl Complexes via High-Valent Pd Intermediates | Organometallics
Palladium-catalyzed reaction of γ-silylated allyl acetates proceeding through 1,2-shift of a substituent on silicon - ScienceDirect
Palladium‐Catalyzed Allylic Substitution at Four‐Membered‐Ring Systems: Formation of η1‐Allyl Complexes and Electrocyclic Ring Opening - Audisio - 2013 - Angewandte Chemie International Edition - Wiley Online Library
Palladium(II)-Catalyzed Regioselective Hydroesterification of 1,3-Conjugated Enynes with Aryl Formates | Organic Letters
Palladium-catalyzed reaction of γ-silylated allyl acetates proceeding through 1,2-shift of a substituent on silicon - ScienceDirect
