![Aqueous-Phase Chemistry of η3-Allylpalladium(II) Complexes with Sulfonated N-Heterocyclic Carbene Ligands: Solvent Effects in the Protolysis of Pd–C Bonds and Suzuki–Miyaura Reactions - Organometallics - X-MOL Aqueous-Phase Chemistry of η3-Allylpalladium(II) Complexes with Sulfonated N-Heterocyclic Carbene Ligands: Solvent Effects in the Protolysis of Pd–C Bonds and Suzuki–Miyaura Reactions - Organometallics - X-MOL](https://xpic.x-mol.com/20171021%2F10.1021_acs.organomet.7b00635.jpg)
Aqueous-Phase Chemistry of η3-Allylpalladium(II) Complexes with Sulfonated N-Heterocyclic Carbene Ligands: Solvent Effects in the Protolysis of Pd–C Bonds and Suzuki–Miyaura Reactions - Organometallics - X-MOL
![Synthesis and characterization of (π-allyl)palladium(II) complexes containing dialkylbiaryl phosphine ligands - ScienceDirect Synthesis and characterization of (π-allyl)palladium(II) complexes containing dialkylbiaryl phosphine ligands - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0277538715006592-gr7.jpg)
Synthesis and characterization of (π-allyl)palladium(II) complexes containing dialkylbiaryl phosphine ligands - ScienceDirect
![Report: Palladium(I) and Nickel(I) Bridging Allyl Dimers for the Catalytic Functionalization of CO2 (58th Annual Report on Research Under Sponsorship of The American Chemical Society Petroleum Research Fund) Report: Palladium(I) and Nickel(I) Bridging Allyl Dimers for the Catalytic Functionalization of CO2 (58th Annual Report on Research Under Sponsorship of The American Chemical Society Petroleum Research Fund)](https://acswebcontent.acs.org/prfar/2013/images/Paper_12241_abstract_20059_0.jpg)
Report: Palladium(I) and Nickel(I) Bridging Allyl Dimers for the Catalytic Functionalization of CO2 (58th Annual Report on Research Under Sponsorship of The American Chemical Society Petroleum Research Fund)
A Mechanistic Study of Direct Activation of Allylic Alcohols in Palladium Catalyzed Amination Reactions
![Stereochemistry of the palladium-catalyzed allylic substitution: the syn-anti dichotomy in the formation of (π-allyl)palladium complexes and their equilibration - ScienceDirect Stereochemistry of the palladium-catalyzed allylic substitution: the syn-anti dichotomy in the formation of (π-allyl)palladium complexes and their equilibration - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0040402001882636-gr1.gif)
Stereochemistry of the palladium-catalyzed allylic substitution: the syn-anti dichotomy in the formation of (π-allyl)palladium complexes and their equilibration - ScienceDirect
![PDF] Confirming the existence of π-allyl-palladium intermediates during the reaction of meta photocycloadducts with palladium(II) compounds. | Semantic Scholar PDF] Confirming the existence of π-allyl-palladium intermediates during the reaction of meta photocycloadducts with palladium(II) compounds. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/e3170611736068557037b936b6641e36bc061f7e/4-Figure2-1.png)
PDF] Confirming the existence of π-allyl-palladium intermediates during the reaction of meta photocycloadducts with palladium(II) compounds. | Semantic Scholar
Catalytic allylic functionalization via π-allyl palladium chemistry - Organic & Biomolecular Chemistry (RSC Publishing)
![Steric Effects in Enantioselective Allylic Alkylation Catalysed by Cationic(η3‐Allyl)palladium Complexes Bearing Chiral Pyridine‐Aziridine Ligands - Ferioli - 2005 - European Journal of Organic Chemistry - Wiley Online Library Steric Effects in Enantioselective Allylic Alkylation Catalysed by Cationic(η3‐Allyl)palladium Complexes Bearing Chiral Pyridine‐Aziridine Ligands - Ferioli - 2005 - European Journal of Organic Chemistry - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/c1e5308e-daa1-4e20-b9af-f300b5fc68ac/mfig000.jpg)
Steric Effects in Enantioselective Allylic Alkylation Catalysed by Cationic(η3‐Allyl)palladium Complexes Bearing Chiral Pyridine‐Aziridine Ligands - Ferioli - 2005 - European Journal of Organic Chemistry - Wiley Online Library
![Palladium/N-heterocyclic carbene catalysed regio and diastereoselective reaction of ketones with allyl reagents via inner-sphere mechanism | Nature Communications Palladium/N-heterocyclic carbene catalysed regio and diastereoselective reaction of ketones with allyl reagents via inner-sphere mechanism | Nature Communications](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fncomms11806/MediaObjects/41467_2016_Article_BFncomms11806_Fig1_HTML.jpg)
Palladium/N-heterocyclic carbene catalysed regio and diastereoselective reaction of ketones with allyl reagents via inner-sphere mechanism | Nature Communications
![Palladium‐Catalyzed Electrophilic Allylation Reactions via Bis(allyl) palladium Complexes and Related Intermediates - Szabó - 2004 - Chemistry – A European 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](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/dfe73890-858a-44fb-9c71-084e44d7d133/msch005.jpg)
Palladium‐Catalyzed Electrophilic Allylation Reactions via Bis(allyl) palladium Complexes and Related Intermediates - Szabó - 2004 - Chemistry – A European Journal - Wiley Online Library
![Synthesis and characterization of (π-allyl)palladium(II) complexes containing dialkylbiaryl phosphine ligands - ScienceDirect Synthesis and characterization of (π-allyl)palladium(II) complexes containing dialkylbiaryl phosphine ligands - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0277538715006592-gr6.jpg)