![Palladium-Catalyzed Synthesis of N-Cyclohexyl Anilines from Phenols with Hydrazine or Hydroxylamine via N-N/O Cleavage - Adv. Synth. Catal. - X-MOL Palladium-Catalyzed Synthesis of N-Cyclohexyl Anilines from Phenols with Hydrazine or Hydroxylamine via N-N/O Cleavage - Adv. Synth. Catal. - X-MOL](https://xpic.x-mol.com/20170908%2F10.1002_adsc.201700712.jpg)
Palladium-Catalyzed Synthesis of N-Cyclohexyl Anilines from Phenols with Hydrazine or Hydroxylamine via N-N/O Cleavage - Adv. Synth. Catal. - X-MOL
![Palladium‐Catalyzed Asymmetric Amination of Allenyl Phosphates: Enantioselective Synthesis of Allenes with an Additional Unsaturated Unit - Li - 2014 - Angewandte Chemie International Edition - Wiley Online Library Palladium‐Catalyzed Asymmetric Amination of Allenyl Phosphates: Enantioselective Synthesis of Allenes with an Additional Unsaturated Unit - Li - 2014 - Angewandte Chemie International Edition - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/b3e485dc-61ec-4ea6-97d3-d7127a120b04/mcontent.jpg)
Palladium‐Catalyzed Asymmetric Amination of Allenyl Phosphates: Enantioselective Synthesis of Allenes with an Additional Unsaturated Unit - Li - 2014 - Angewandte Chemie International Edition - Wiley Online Library
![Cyclization of Bisphosphines to Phosphacycles via the Cleavage of Two Carbon–Phosphorus Bonds by Nickel Catalysis,Organic Letters - X-MOL Cyclization of Bisphosphines to Phosphacycles via the Cleavage of Two Carbon–Phosphorus Bonds by Nickel Catalysis,Organic Letters - X-MOL](https://xpic.x-mol.com/20190525%2F10.1021_acs.orglett.9b01355.jpg)
Cyclization of Bisphosphines to Phosphacycles via the Cleavage of Two Carbon–Phosphorus Bonds by Nickel Catalysis,Organic Letters - X-MOL
![Enantioselective Decarboxylative Amination: Synthesis of Axially Chiral Allenyl Amines - Wan - 2013 - Angewandte Chemie International Edition - Wiley Online Library Enantioselective Decarboxylative Amination: Synthesis of Axially Chiral Allenyl Amines - Wan - 2013 - Angewandte Chemie International Edition - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/408bd954-f671-4289-97de-4995b33c24da/mcontent.jpg)
Enantioselective Decarboxylative Amination: Synthesis of Axially Chiral Allenyl Amines - Wan - 2013 - Angewandte Chemie International Edition - Wiley Online Library
![Palladium‐Catalyzed Cascade C−O Cleavage and C−H Alkenylation of Phosphinyl Allenes: An Expeditious Approach to 3‐Alkenyl Benzo[b]phosphole Oxides - Liu - 2018 - Advanced Synthesis & Catalysis - Wiley Online Library Palladium‐Catalyzed Cascade C−O Cleavage and C−H Alkenylation of Phosphinyl Allenes: An Expeditious Approach to 3‐Alkenyl Benzo[b]phosphole Oxides - Liu - 2018 - Advanced Synthesis & Catalysis - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/b48782c2-6140-4825-86be-d0da17165f14/adsc201800103-toc-0001-m.jpg)
Palladium‐Catalyzed Cascade C−O Cleavage and C−H Alkenylation of Phosphinyl Allenes: An Expeditious Approach to 3‐Alkenyl Benzo[b]phosphole Oxides - Liu - 2018 - Advanced Synthesis & Catalysis - Wiley Online Library
![Intramolecular C–F and C–H bond cleavage promoted by butadienyl heavy Grignard reagents | Nature Communications Intramolecular C–F and C–H bond cleavage promoted by butadienyl heavy Grignard reagents | Nature Communications](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fncomms5508/MediaObjects/41467_2014_Article_BFncomms5508_Fig5_HTML.jpg)
Intramolecular C–F and C–H bond cleavage promoted by butadienyl heavy Grignard reagents | Nature Communications
![Palladium: Organometallic Chemistry - William Suggs - - Major Reference Works - Wiley Online Library Palladium: Organometallic Chemistry - William Suggs - - Major Reference Works - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/ad832762-8b76-4023-b2e8-7b5e09dd1cb7/nsc019.gif)
Palladium: Organometallic Chemistry - William Suggs - - Major Reference Works - Wiley Online Library
![Three Carbons for Complexity! Recent Developments of Palladium‐Catalyzed Reactions of Allenes - Lechel - 2013 - ChemCatChem - Wiley Online Library Three Carbons for Complexity! Recent Developments of Palladium‐Catalyzed Reactions of Allenes - Lechel - 2013 - ChemCatChem - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/2111f803-28de-4b26-90fa-643728b4f39b/msch002.gif)
Three Carbons for Complexity! Recent Developments of Palladium‐Catalyzed Reactions of Allenes - Lechel - 2013 - ChemCatChem - Wiley Online Library
![Unusual C–O bond cleavage of aromatic ethers in ruthenium complexes bearing a 2-alkoxypyridyl fragment† - Dalton Trans. - X-MOL Unusual C–O bond cleavage of aromatic ethers in ruthenium complexes bearing a 2-alkoxypyridyl fragment† - Dalton Trans. - X-MOL](https://xpic.x-mol.com/20190918%2F10.1039_C9DT03020D.jpg)
Unusual C–O bond cleavage of aromatic ethers in ruthenium complexes bearing a 2-alkoxypyridyl fragment† - Dalton Trans. - X-MOL
![Facile and selective cleavage of allyl ethers, amines and esters using polymethylhydrosiloxane-ZnCl2/Pd(PPh3)4 Facile and selective cleavage of allyl ethers, amines and esters using polymethylhydrosiloxane-ZnCl2/Pd(PPh3)4](https://www.organic-chemistry.org/abstracts/literature/763m.gif)
Facile and selective cleavage of allyl ethers, amines and esters using polymethylhydrosiloxane-ZnCl2/Pd(PPh3)4
![Propargylic C(sp3)–H Bond Activation for Preparing η3-Propargyl/Allenyl Complexes of Yttrium,Organometallics - X-MOL Propargylic C(sp3)–H Bond Activation for Preparing η3-Propargyl/Allenyl Complexes of Yttrium,Organometallics - X-MOL](https://xpic.x-mol.com/20170817%2F10.1021_acs.organomet.7b00395.jpg)
Propargylic C(sp3)–H Bond Activation for Preparing η3-Propargyl/Allenyl Complexes of Yttrium,Organometallics - X-MOL
![Palladium-Catalyzed Cleavage of α-Allenylic Aryl Ether toward Pyrazolemethylene-Substituted Phosphinyl Allenes and Their Transformations via Alkenyl C–P(O) Cleavage - Org. Lett. - X-MOL Palladium-Catalyzed Cleavage of α-Allenylic Aryl Ether toward Pyrazolemethylene-Substituted Phosphinyl Allenes and Their Transformations via Alkenyl C–P(O) Cleavage - Org. Lett. - X-MOL](https://xpic.x-mol.com/thesis%2FOrganic_Letters%2Fol-2017-002137_0006.gif)
Palladium-Catalyzed Cleavage of α-Allenylic Aryl Ether toward Pyrazolemethylene-Substituted Phosphinyl Allenes and Their Transformations via Alkenyl C–P(O) Cleavage - Org. Lett. - X-MOL
Palladium-Catalyzed Cleavage of α-Allenylic Aryl Ether toward Pyrazolemethylene-Substituted Phosphinyl Allenes and Their Transf
![Facile and selective cleavage of allyl ethers, amines and esters using polymethylhydrosiloxane-ZnCl2/Pd(PPh3)4 Facile and selective cleavage of allyl ethers, amines and esters using polymethylhydrosiloxane-ZnCl2/Pd(PPh3)4](https://www.organic-chemistry.org/abstracts/literature/763b.gif)
Facile and selective cleavage of allyl ethers, amines and esters using polymethylhydrosiloxane-ZnCl2/Pd(PPh3)4
![Molecules | Free Full-Text | The Heck Reaction Applied to 1,3- and 1,2-Unsaturated Derivatives, a Way towards Molecular Complexity | HTML Molecules | Free Full-Text | The Heck Reaction Applied to 1,3- and 1,2-Unsaturated Derivatives, a Way towards Molecular Complexity | HTML](https://www.mdpi.com/molecules/molecules-15-02667/article_deploy/html/images/molecules-15-02667-g029.png)
Molecules | Free Full-Text | The Heck Reaction Applied to 1,3- and 1,2-Unsaturated Derivatives, a Way towards Molecular Complexity | HTML
![Intramolecular C–F and C–H bond cleavage promoted by butadienyl heavy Grignard reagents | Nature Communications Intramolecular C–F and C–H bond cleavage promoted by butadienyl heavy Grignard reagents | Nature Communications](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fncomms5508/MediaObjects/41467_2014_Article_BFncomms5508_Fig1_HTML.jpg)
Intramolecular C–F and C–H bond cleavage promoted by butadienyl heavy Grignard reagents | Nature Communications
![Mechanistic insights into transition metal-mediated bioorthogonal uncaging reactions - Chemical Society Reviews (RSC Publishing) Mechanistic insights into transition metal-mediated bioorthogonal uncaging reactions - Chemical Society Reviews (RSC Publishing)](https://pubs.rsc.org/image/article/2020/cs/d0cs00630k/d0cs00630k-s9_hi-res.gif)