![Pd-Catalyzed Debenzylation and Deallylation of Ethers and Esters with Sodium Hydride - ACS Catal. - X-MOL Pd-Catalyzed Debenzylation and Deallylation of Ethers and Esters with Sodium Hydride - ACS Catal. - X-MOL](https://xpic.x-mol.com/20180309%2F10.1021_acscatal.8b00185.jpg)
Pd-Catalyzed Debenzylation and Deallylation of Ethers and Esters with Sodium Hydride - ACS Catal. - X-MOL
![Palladium-Catalyzed Synthesis of Substituted Cycloheptane-1,4-diones by an Asymmetric Ring-Expanding Allylation (AREA) Palladium-Catalyzed Synthesis of Substituted Cycloheptane-1,4-diones by an Asymmetric Ring-Expanding Allylation (AREA)](https://atomchuxky.files.wordpress.com/2007/04/114.jpg?w=317)
Palladium-Catalyzed Synthesis of Substituted Cycloheptane-1,4-diones by an Asymmetric Ring-Expanding Allylation (AREA)
![Palladium-Mediated Dealkylation of N -Propargyl-Floxuridine as a Bioorthogonal Oxygen-Independent Prodrug Strategy | Scientific Reports Palladium-Mediated Dealkylation of N -Propargyl-Floxuridine as a Bioorthogonal Oxygen-Independent Prodrug Strategy | Scientific Reports](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fsrep09329/MediaObjects/41598_2015_Article_BFsrep09329_Fig1_HTML.jpg)
Palladium-Mediated Dealkylation of N -Propargyl-Floxuridine as a Bioorthogonal Oxygen-Independent Prodrug Strategy | Scientific Reports
![Direct C–N bond cleavage of N-vinyl or N-allyl arylamines: a metal-free strategy for N-devinylation and N-deallylation - Tetrahedron Lett. - X-MOL Direct C–N bond cleavage of N-vinyl or N-allyl arylamines: a metal-free strategy for N-devinylation and N-deallylation - Tetrahedron Lett. - X-MOL](https://xpic.x-mol.com/thesis%2FTetrahedron_Letters%2F1-s2.0-S0040403915008515-fx1.jpg.jpeg)
Direct C–N bond cleavage of N-vinyl or N-allyl arylamines: a metal-free strategy for N-devinylation and N-deallylation - Tetrahedron Lett. - X-MOL
![Palladium‐Catalyzed Oxidative Sulfamidation: A Stereoselective Synthesis for Enesulfonamides - Panda - 2017 - Advanced Synthesis & Catalysis - Wiley Online Library Palladium‐Catalyzed Oxidative Sulfamidation: A Stereoselective Synthesis for Enesulfonamides - Panda - 2017 - Advanced Synthesis & Catalysis - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/0146a991-a563-4a4e-8ae2-ceef3f9dca9e/adsc201601048-toc-0001-m.jpg)
Palladium‐Catalyzed Oxidative Sulfamidation: A Stereoselective Synthesis for Enesulfonamides - Panda - 2017 - Advanced Synthesis & Catalysis - Wiley Online Library
Palladium-Catalyzed Oxidative N-Dealkylation/Carbonylation of Tertiary Amines with Alkynes to α,β-Alkynylamides
![Direct activation of relatively unstrained carbon–carbon bonds in homogeneous systems - Organic Chemistry Frontiers (RSC Publishing) DOI:10.1039/C4QO00053F Direct activation of relatively unstrained carbon–carbon bonds in homogeneous systems - Organic Chemistry Frontiers (RSC Publishing) DOI:10.1039/C4QO00053F](https://pubs.rsc.org/image/article/2014/QO/c4qo00053f/c4qo00053f-s11_hi-res.gif)
Direct activation of relatively unstrained carbon–carbon bonds in homogeneous systems - Organic Chemistry Frontiers (RSC Publishing) DOI:10.1039/C4QO00053F
![Elaboration of the ether cleaving ability and selectivity of the classical Pearlman's catalyst [Pd(OH)2/C]: concise synthesis of a precursor for a myo-inositol pyrophosphate - ScienceDirect Elaboration of the ether cleaving ability and selectivity of the classical Pearlman's catalyst [Pd(OH)2/C]: concise synthesis of a precursor for a myo-inositol pyrophosphate - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0040402012013944-sc6.jpg)
Elaboration of the ether cleaving ability and selectivity of the classical Pearlman's catalyst [Pd(OH)2/C]: concise synthesis of a precursor for a myo-inositol pyrophosphate - ScienceDirect
![Catalysts | Free Full-Text | PdI2-Based Catalysis for Carbonylation Reactions: A Personal Account | HTML Catalysts | Free Full-Text | PdI2-Based Catalysis for Carbonylation Reactions: A Personal Account | HTML](https://www.mdpi.com/catalysts/catalysts-09-00610/article_deploy/html/images/catalysts-09-00610-sch040.png)
Catalysts | Free Full-Text | PdI2-Based Catalysis for Carbonylation Reactions: A Personal Account | HTML
![Noneffervescent Method for Catalysis-Based Palladium Detection with Color or Fluorescence,ACS Sensors - X-MOL Noneffervescent Method for Catalysis-Based Palladium Detection with Color or Fluorescence,ACS Sensors - X-MOL](https://xpic.x-mol.com/20171024%2F10.1021_acssensors.7b00697.jpg)
Noneffervescent Method for Catalysis-Based Palladium Detection with Color or Fluorescence,ACS Sensors - X-MOL
![Triphenylphosphine-assisted highly sensitive fluorescent chemosensor for ratiometric detection of palladium in solution and living cells - RSC Advances (RSC Publishing) Triphenylphosphine-assisted highly sensitive fluorescent chemosensor for ratiometric detection of palladium in solution and living cells - RSC Advances (RSC Publishing)](https://pubs.rsc.org/image/article/2015/ra/c5ra17819c/c5ra17819c-s2_hi-res.gif)
Triphenylphosphine-assisted highly sensitive fluorescent chemosensor for ratiometric detection of palladium in solution and living cells - RSC Advances (RSC Publishing)
![Extracellular palladium-catalysed dealkylation of 5-fluoro-1-propargyl-uracil as a bioorthogonally activated prodrug approach | Nature Communications Extracellular palladium-catalysed dealkylation of 5-fluoro-1-propargyl-uracil as a bioorthogonally activated prodrug approach | Nature Communications](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fncomms4277/MediaObjects/41467_2014_Article_BFncomms4277_Fig1_HTML.jpg)
Extracellular palladium-catalysed dealkylation of 5-fluoro-1-propargyl-uracil as a bioorthogonally activated prodrug approach | Nature Communications
![Hydrolytic Deallylation of N‐Allyl Amides Catalyzed by PdII Complexes - Ohmura - 2008 - European Journal of Organic Chemistry - Wiley Online Library Hydrolytic Deallylation of N‐Allyl Amides Catalyzed by PdII Complexes - Ohmura - 2008 - European Journal of Organic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/c72831cc-47e3-4533-8503-4a99c5e1326d/mscheme3.jpg)
Hydrolytic Deallylation of N‐Allyl Amides Catalyzed by PdII Complexes - Ohmura - 2008 - European Journal of Organic Chemistry - Wiley Online Library
![Application of a new phosphorus-free palladium heterogeneous nanocatalyst supported on modified MWCNT the highly selective and efficient cleavage of propargyl, allyl, and benzyl phenol ethers under mild conditions | SpringerLink Application of a new phosphorus-free palladium heterogeneous nanocatalyst supported on modified MWCNT the highly selective and efficient cleavage of propargyl, allyl, and benzyl phenol ethers under mild conditions | SpringerLink](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs11030-015-9585-3/MediaObjects/11030_2015_9585_Sch2_HTML.gif)
Application of a new phosphorus-free palladium heterogeneous nanocatalyst supported on modified MWCNT the highly selective and efficient cleavage of propargyl, allyl, and benzyl phenol ethers under mild conditions | SpringerLink
![N-allyl-N-sulfonyl ynamides as synthetic precursors to amidines and vinylogous amidines. An unexpected N-to-C 1,3-sulfonyl shift in nitrile synthesis. - Abstract - Europe PMC N-allyl-N-sulfonyl ynamides as synthetic precursors to amidines and vinylogous amidines. An unexpected N-to-C 1,3-sulfonyl shift in nitrile synthesis. - Abstract - Europe PMC](https://europepmc.org/articles/PMC3120114/bin/nihms296704f10.jpg)