Catalytic allylic functionalization via π-allyl palladium chemistry - Organic & Biomolecular Chemistry (RSC Publishing)
![Asymmetric allylic substitution by chiral palladium catalysts: Which is more reactive, major π-allyl Pd(II) species or minor π-allyl species? - ScienceDirect Asymmetric allylic substitution by chiral palladium catalysts: Which is more reactive, major π-allyl Pd(II) species or minor π-allyl species? - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S2468823120304843-ga1.jpg)
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 reaction of γ-silylated allyl acetates proceeding through 1,2-shift of a substituent on silicon - ScienceDirect Palladium-catalyzed reaction of γ-silylated allyl acetates proceeding through 1,2-shift of a substituent on silicon - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0040402020306773-sc1.jpg)
Palladium-catalyzed reaction of γ-silylated allyl acetates proceeding through 1,2-shift of a substituent on silicon - ScienceDirect
![Relative Rates for the Amination of η3-Allyl and η3-Benzyl Complexes of Palladium | Journal of the American Chemical Society Relative Rates for the Amination of η3-Allyl and η3-Benzyl Complexes of Palladium | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/ja067084h/asset/images/medium/ja067084hn00001.gif)
Relative Rates for the Amination of η3-Allyl and η3-Benzyl Complexes of Palladium | Journal of the American Chemical Society
![Palladium-catalyzed reaction of γ-silylated allyl acetates proceeding through 1,2-shift of a substituent on silicon - ScienceDirect Palladium-catalyzed reaction of γ-silylated allyl acetates proceeding through 1,2-shift of a substituent on silicon - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0040402020306773-sc2.jpg)
Palladium-catalyzed reaction of γ-silylated allyl acetates proceeding through 1,2-shift of a substituent on silicon - ScienceDirect
![PDF) Palladium complexes with a tridentate PNO ligand. Synthesis of ??1- allyl complexes and cross-coupling reactions promoted by boron compounds PDF) Palladium complexes with a tridentate PNO ligand. Synthesis of ??1- allyl complexes and cross-coupling reactions promoted by boron compounds](https://i1.rgstatic.net/publication/42768797_Palladium_complexes_with_a_tridentate_PNO_ligand_Synthesis_of_1-allyl_complexes_and_cross-coupling_reactions_promoted_by_boron_compounds/links/5702330e08ae1408e15eb1fe/largepreview.png)
PDF) Palladium complexes with a tridentate PNO ligand. Synthesis of ??1- allyl complexes and cross-coupling reactions promoted by boron compounds
![Catalysts | Free Full-Text | Synthesis, Characterization, Solution Behavior and Theoretical Studies of Pd(II) Allyl Complexes with 2-Phenyl-3H-indoles as Ligands Catalysts | Free Full-Text | Synthesis, Characterization, Solution Behavior and Theoretical Studies of Pd(II) Allyl Complexes with 2-Phenyl-3H-indoles as Ligands](https://pub.mdpi-res.com/catalysts/catalysts-09-00811/article_deploy/html/images/catalysts-09-00811-ag-550.jpg?1572350724)
Catalysts | Free Full-Text | Synthesis, Characterization, Solution Behavior and Theoretical Studies of Pd(II) Allyl Complexes with 2-Phenyl-3H-indoles as Ligands
Relative Rates for the Amination of η3-Allyl and η3-Benzyl Complexes of Palladium | Journal of the American Chemical Society
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
![Palladium‐Catalyzed Allyl Cross‐Coupling Reactions with In Situ Generated Organoindium Reagents - Lee - 2011 - Chemistry – An Asian 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](https://onlinelibrary.wiley.com/cms/asset/07b08ddc-9fde-43be-8bc1-f46b23e7f177/mcontent.gif)
Palladium‐Catalyzed Allyl Cross‐Coupling Reactions with In Situ Generated Organoindium Reagents - Lee - 2011 - Chemistry – An Asian Journal - Wiley Online Library
![Protonation of palladium(II)-allyl and palladium(0)-olefin complexes containing 2-pyridyldiphenylphosphine - ScienceDirect Protonation of palladium(II)-allyl and palladium(0)-olefin complexes containing 2-pyridyldiphenylphosphine - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0022328X08006281-fx1.jpg)
Protonation of palladium(II)-allyl and palladium(0)-olefin complexes containing 2-pyridyldiphenylphosphine - ScienceDirect
![Formation of Palladium(0) Complexes from Pd(OAc)2 and a Bidentate Phosphine Ligand (dppp) and Their Reactivity in Oxidative Addition | Organometallics Formation of Palladium(0) Complexes from Pd(OAc)2 and a Bidentate Phosphine Ligand (dppp) and Their Reactivity in Oxidative Addition | Organometallics](https://pubs.acs.org/cms/10.1021/om0101137/asset/images/large/om0101137n00001.jpeg)
Formation of Palladium(0) Complexes from Pd(OAc)2 and a Bidentate Phosphine Ligand (dppp) and Their Reactivity in Oxidative Addition | Organometallics
![Synergistic Organoboron/Palladium Catalysis for Regioselective N-Allylations of Azoles with Allylic Alcohols | Organic Letters Synergistic Organoboron/Palladium Catalysis for Regioselective N-Allylations of Azoles with Allylic Alcohols | Organic Letters](https://pubs.acs.org/cms/10.1021/acs.orglett.2c03084/asset/images/large/ol2c03084_0005.jpeg)
Synergistic Organoboron/Palladium Catalysis for Regioselective N-Allylations of Azoles with Allylic Alcohols | Organic Letters
![Development, Mechanism, and Scope of the Palladium-Catalyzed Enantioselective Allene Diboration | Journal of the American Chemical Society Development, Mechanism, and Scope of the Palladium-Catalyzed Enantioselective Allene Diboration | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/ja070572k/asset/images/large/ja070572kn00001.jpeg)
Development, Mechanism, and Scope of the Palladium-Catalyzed Enantioselective Allene Diboration | Journal of the American Chemical Society
![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/4e59bbce-9d2a-4ed0-aa89-363f4491ef6b/msch013.jpg)
Palladium‐Catalyzed Electrophilic Allylation Reactions via Bis(allyl) palladium Complexes and Related Intermediates - Szabó - 2004 - Chemistry – A European Journal - Wiley Online Library
![Palladium -catalyzed tetraallylation of C 60 with allyl chloride and allylstannane : mechanism, regioselectivity, and enantioselectivity - Chemical Science (RSC Publishing) DOI:10.1039/C2SC21126B Palladium -catalyzed tetraallylation of C 60 with allyl chloride and allylstannane : mechanism, regioselectivity, and enantioselectivity - Chemical Science (RSC Publishing) DOI:10.1039/C2SC21126B](https://pubs.rsc.org/image/article/2012/SC/c2sc21126b/c2sc21126b-s2.gif)
Palladium -catalyzed tetraallylation of C 60 with allyl chloride and allylstannane : mechanism, regioselectivity, and enantioselectivity - Chemical Science (RSC Publishing) DOI:10.1039/C2SC21126B
![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/948b74e6-f1f2-454f-a6c2-cdb2a32ea5e4/msch001.jpg)
Palladium‐Catalyzed Electrophilic Allylation Reactions via Bis(allyl) palladium Complexes and Related Intermediates - Szabó - 2004 - Chemistry – A European Journal - Wiley Online Library
Mechanism of the η3−η1−η3 Isomerization in Allylpalladium Complexes: Solvent Coordination, Ligand, and Substituent Effects | Organometallics
![Recent development of allyl–allyl cross-coupling and its application in natural product synthesis - Organic Chemistry Frontiers (RSC Publishing) DOI:10.1039/D2QO01078J Recent development of allyl–allyl cross-coupling and its application in natural product synthesis - Organic Chemistry Frontiers (RSC Publishing) DOI:10.1039/D2QO01078J](https://pubs.rsc.org/image/article/2023/QO/d2qo01078j/d2qo01078j-s4_hi-res.gif)
Recent development of allyl–allyl cross-coupling and its application in natural product synthesis - Organic Chemistry Frontiers (RSC Publishing) DOI:10.1039/D2QO01078J
Generating Active “L-Pd(0)” via Neutral or Cationic π-Allylpalladium Complexes Featuring Biaryl/Bipyrazolylphosphines: Synthetic, Mechanistic, and Structure–Activity Studies in Challenging Cross-Coupling Reactions | The Journal of Organic Chemistry
Effect of 2-Substituents on Allyl-Supported Precatalysts for the Suzuki–Miyaura Reaction: Relating Catalytic Efficiency to the Stability of Palladium(I) Bridging Allyl Dimers | Organometallics
![Palladium-catalyzed reaction of γ-silylated allyl acetates proceeding through 1,2-shift of a substituent on silicon - ScienceDirect Palladium-catalyzed reaction of γ-silylated allyl acetates proceeding through 1,2-shift of a substituent on silicon - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0040402020306773-fx1.jpg)
Palladium-catalyzed reaction of γ-silylated allyl acetates proceeding through 1,2-shift of a substituent on silicon - ScienceDirect
![Palladium‐Catalyzed Allyl Cross‐Coupling Reactions with In Situ Generated Organoindium Reagents - Lee - 2011 - Chemistry – An Asian 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](https://onlinelibrary.wiley.com/cms/asset/01901fea-0f53-49b6-89d3-634f1cfdaf6f/msch001.jpg)
Palladium‐Catalyzed Allyl Cross‐Coupling Reactions with In Situ Generated Organoindium Reagents - Lee - 2011 - Chemistry – An Asian Journal - Wiley Online Library
![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‐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](https://onlinelibrary.wiley.com/cms/asset/3e852902-17c0-4020-be4e-9d6526a6ccc9/mcontent.jpg)
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
![Scheme 3. Part of the mechanism for the palladium catalyzed allylic... | Download Scientific Diagram Scheme 3. Part of the mechanism for the palladium catalyzed allylic... | Download Scientific Diagram](https://www.researchgate.net/publication/336111774/figure/fig1/AS:807909067862016@1569631940099/Scheme-3-Part-of-the-mechanism-for-the-palladium-catalyzed-allylic-alkylation-of.png)