![Molecules | Free Full-Text | Palladium and Organocatalysis: An Excellent Recipe for Asymmetric Synthesis Molecules | Free Full-Text | Palladium and Organocatalysis: An Excellent Recipe for Asymmetric Synthesis](https://www.mdpi.com/molecules/molecules-18-10108/article_deploy/html/images/molecules-18-10108-g001.png)
Molecules | Free Full-Text | Palladium and Organocatalysis: An Excellent Recipe for Asymmetric Synthesis
![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
![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
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(II)-Catalyzed Regioselective Hydroesterification of 1,3-Conjugated Enynes with Aryl Formates | Organic Letters Palladium(II)-Catalyzed Regioselective Hydroesterification of 1,3-Conjugated Enynes with Aryl Formates | Organic Letters](https://pubs.acs.org/cms/10.1021/acs.orglett.2c04103/asset/images/large/ol2c04103_0008.jpeg)
Palladium(II)-Catalyzed Regioselective Hydroesterification of 1,3-Conjugated Enynes with Aryl Formates | Organic Letters
![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
![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](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
![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/df48276a-99ff-42df-8602-09a824ec0b6f/msch009.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 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
![Palladium-Catalyzed, Site-Selective Direct Allylation of Aryl C–H Bonds by Silver-Mediated C–H Activation: A Synthetic and Mechanistic Investigation | Journal of the American Chemical Society Palladium-Catalyzed, Site-Selective Direct Allylation of Aryl C–H Bonds by Silver-Mediated C–H Activation: A Synthetic and Mechanistic Investigation | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/jacs.6b10220/asset/images/large/ja-2016-102209_0020.jpeg)
Palladium-Catalyzed, Site-Selective Direct Allylation of Aryl C–H Bonds by Silver-Mediated C–H Activation: A Synthetic and Mechanistic Investigation | Journal of the American Chemical Society
![PDF) Heterolytic Splitting of Allylic Alcohols with Palladium(0)−TPPTS in Water. Stabilities of the Allylphosphonium Salt of TPPTS and of the Ionic Complex [Pd(η 3 -allyl)(TPPTS) 2 ] + PDF) Heterolytic Splitting of Allylic Alcohols with Palladium(0)−TPPTS in Water. Stabilities of the Allylphosphonium Salt of TPPTS and of the Ionic Complex [Pd(η 3 -allyl)(TPPTS) 2 ] +](https://www.researchgate.net/profile/Iyad-Karame/publication/244460612/figure/fig6/AS:671187042566145@1537034869190/Allyl-alcohol-reaction-without-acid-addition-pH-versus-time-Conditions-Pd-00055-M_Q320.jpg)
PDF) Heterolytic Splitting of Allylic Alcohols with Palladium(0)−TPPTS in Water. Stabilities of the Allylphosphonium Salt of TPPTS and of the Ionic Complex [Pd(η 3 -allyl)(TPPTS) 2 ] +
![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
![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)
Scheme 3. Part of the mechanism for the palladium catalyzed allylic... | Download Scientific Diagram
![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](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
![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
![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/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
Relative Rates for the Amination of η3-Allyl and η3-Benzyl Complexes of Palladium | Journal of the American Chemical Society
![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 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
Mechanism of the η3−η1−η3 Isomerization in Allylpalladium Complexes: Solvent Coordination, Ligand, and Substituent Effects | Organometallics
![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
![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
![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
Catalytic allylic functionalization via π-allyl palladium chemistry - Organic & Biomolecular Chemistry (RSC Publishing)
![Palladium(I)-Bridging Allyl Dimers for the Catalytic Functionalization of CO2 | Journal of the American Chemical Society Palladium(I)-Bridging Allyl Dimers for the Catalytic Functionalization of CO2 | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/ja110708k/asset/images/medium/ja-2010-10708k_0010.gif)