![1499115-56-8・Diphenyl Phenanthroline NNC Palladium [DPP-NNC Pd]・044-34351・040-34353[Detail Information] | [Synthesis & Materials] |Laboratory Chemicals-FUJIFILM Wako Chemicals U.S.A. Corporation 1499115-56-8・Diphenyl Phenanthroline NNC Palladium [DPP-NNC Pd]・044-34351・040-34353[Detail Information] | [Synthesis & Materials] |Laboratory Chemicals-FUJIFILM Wako Chemicals U.S.A. Corporation](https://labchem-wako.fujifilm.com/sc/01/1499115-56-8.png)
1499115-56-8・Diphenyl Phenanthroline NNC Palladium [DPP-NNC Pd]・044-34351・040-34353[Detail Information] | [Synthesis & Materials] |Laboratory Chemicals-FUJIFILM Wako Chemicals U.S.A. Corporation
![Synthesis of Indoles by Intermolecular Cyclization of Unfunctionalized Nitroarenes and Alkynes: One‐Step Synthesis of the Skeleton of Fluvastatin - Ragaini - 2009 - European Journal of Organic Chemistry - Wiley Online Library Synthesis of Indoles by Intermolecular Cyclization of Unfunctionalized Nitroarenes and Alkynes: One‐Step Synthesis of the Skeleton of Fluvastatin - Ragaini - 2009 - European Journal of Organic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/0c4176ec-d4c6-4a54-9d93-1a37b17f054a/mfig000.jpg)
Synthesis of Indoles by Intermolecular Cyclization of Unfunctionalized Nitroarenes and Alkynes: One‐Step Synthesis of the Skeleton of Fluvastatin - Ragaini - 2009 - European Journal of Organic Chemistry - Wiley Online Library
Synthesis, Characterization, and Antibacterial Activities of 1H-Imidazo [5, 6-f] [1,10] Phenanthroline-2(3H)-Thione and Its Ni(II) and Cu(II) Complexes
![1,10‐Phenanthroline Carboxylic Acids for Preparation of Functionalized Metal‐Organic Frameworks - Asian J. Org. Chem. - X-MOL 1,10‐Phenanthroline Carboxylic Acids for Preparation of Functionalized Metal‐Organic Frameworks - Asian J. Org. Chem. - X-MOL](https://xpic.x-mol.com/20191017%2F10.1002_ajoc.201900569.jpg)
1,10‐Phenanthroline Carboxylic Acids for Preparation of Functionalized Metal‐Organic Frameworks - Asian J. Org. Chem. - X-MOL
![Recent Advances in the Palladium Catalyzed Suzuki–Miyaura Cross-Coupling Reaction in Water | SpringerLink Recent Advances in the Palladium Catalyzed Suzuki–Miyaura Cross-Coupling Reaction in Water | SpringerLink](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs10562-016-1707-8/MediaObjects/10562_2016_1707_Sch16_HTML.gif)
Recent Advances in the Palladium Catalyzed Suzuki–Miyaura Cross-Coupling Reaction in Water | SpringerLink
![Palladium‐Catalyzed Intramolecular Cyclization of Nitroalkenes: Synthesis of Thienopyrroles - El‐Atawy - 2017 - European Journal of Organic Chemistry - Wiley Online Library Palladium‐Catalyzed Intramolecular Cyclization of Nitroalkenes: Synthesis of Thienopyrroles - El‐Atawy - 2017 - European Journal of Organic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/46435eaf-39f6-4861-b774-c50279581871/ejoc201700165-toc-0001-m.jpg)
Palladium‐Catalyzed Intramolecular Cyclization of Nitroalkenes: Synthesis of Thienopyrroles - El‐Atawy - 2017 - European Journal of Organic Chemistry - Wiley Online Library
![Platinum(II) and Palladium(II) complexes with 1,10-phenanthroline and pyrrolidinedithiocarbamato ligands: synthesis, DNA-binding and anti-tumor activity in leukemia K562 cell lines | Semantic Scholar Platinum(II) and Palladium(II) complexes with 1,10-phenanthroline and pyrrolidinedithiocarbamato ligands: synthesis, DNA-binding and anti-tumor activity in leukemia K562 cell lines | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/15ded8573fc1d23643e3ee67faf388de8481b0e3/4-Figure1-1.png)
Platinum(II) and Palladium(II) complexes with 1,10-phenanthroline and pyrrolidinedithiocarbamato ligands: synthesis, DNA-binding and anti-tumor activity in leukemia K562 cell lines | Semantic Scholar
![Highly active palladium catalysts containing a 1,10-phenanthroline analogue N-heterocyclic carbene for room temperature Suzuki-Miyaura coupling reactions of aryl chlorides with arylboronic acids in aqueous media - ScienceDirect Highly active palladium catalysts containing a 1,10-phenanthroline analogue N-heterocyclic carbene for room temperature Suzuki-Miyaura coupling reactions of aryl chlorides with arylboronic acids in aqueous media - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0040403916317269-fx1.jpg)
Highly active palladium catalysts containing a 1,10-phenanthroline analogue N-heterocyclic carbene for room temperature Suzuki-Miyaura coupling reactions of aryl chlorides with arylboronic acids in aqueous media - ScienceDirect
![Dichloro (1,10-phenanthroline-5,6-dione) palladium (II) complex supported by mesoporous silica SBA-15 as a photocatalyst for degradation of 2,4-dichlorophenol - ScienceDirect Dichloro (1,10-phenanthroline-5,6-dione) palladium (II) complex supported by mesoporous silica SBA-15 as a photocatalyst for degradation of 2,4-dichlorophenol - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0022286014008540-gr10.jpg)
Dichloro (1,10-phenanthroline-5,6-dione) palladium (II) complex supported by mesoporous silica SBA-15 as a photocatalyst for degradation of 2,4-dichlorophenol - ScienceDirect
![China CAS 14783-10-9 Dichloro (1, 10-phenanthroline) Palladium (II) C12h8cl2n2pd - China Palladium Catalyst, Ruthenium Catalyst China CAS 14783-10-9 Dichloro (1, 10-phenanthroline) Palladium (II) C12h8cl2n2pd - China Palladium Catalyst, Ruthenium Catalyst](https://image.made-in-china.com/2f0j00lHcUIPbBbokq/CAS-14783-10-9-Dichloro-1-10-phenanthroline-Palladium-II-C12h8cl2n2pd.jpg)
China CAS 14783-10-9 Dichloro (1, 10-phenanthroline) Palladium (II) C12h8cl2n2pd - China Palladium Catalyst, Ruthenium Catalyst
![A new method for the reaction of cross-coupling: preparation of 5,5′-bi(1,10-phenanthroline) in: Heterocyclic Communications Volume 23 Issue 1 (2017) A new method for the reaction of cross-coupling: preparation of 5,5′-bi(1,10-phenanthroline) in: Heterocyclic Communications Volume 23 Issue 1 (2017)](https://www.degruyter.com/view/journals/hc/23/1/graphic/j_hc-2016-0225_scheme_001.jpg)
A new method for the reaction of cross-coupling: preparation of 5,5′-bi(1,10-phenanthroline) in: Heterocyclic Communications Volume 23 Issue 1 (2017)
![Design and synthesis of chiral 1,10-phenanthroline ligand, and application in palladium catalyzed asymmetric 1,4-addition reactions - ScienceDirect Design and synthesis of chiral 1,10-phenanthroline ligand, and application in palladium catalyzed asymmetric 1,4-addition reactions - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0040403917310481-fx1.jpg)
Design and synthesis of chiral 1,10-phenanthroline ligand, and application in palladium catalyzed asymmetric 1,4-addition reactions - ScienceDirect
![Chemically deposited palladium nanoparticles on graphene for hydrogen sensor applications | Scientific Reports Chemically deposited palladium nanoparticles on graphene for hydrogen sensor applications | Scientific Reports](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs41598-019-40257-7/MediaObjects/41598_2019_40257_Fig1_HTML.png)
Chemically deposited palladium nanoparticles on graphene for hydrogen sensor applications | Scientific Reports
![14221-01-3・Tetrakis(triphenylphosphine)palladium(0)・209-14643・203-14641[Detail Information] | [Synthesis & Materials] |Laboratory Chemicals-FUJIFILM Wako Chemicals U.S.A. Corporation 14221-01-3・Tetrakis(triphenylphosphine)palladium(0)・209-14643・203-14641[Detail Information] | [Synthesis & Materials] |Laboratory Chemicals-FUJIFILM Wako Chemicals U.S.A. Corporation](https://labchem-wako.fujifilm.com/sc/01/14221-01-3.png)
14221-01-3・Tetrakis(triphenylphosphine)palladium(0)・209-14643・203-14641[Detail Information] | [Synthesis & Materials] |Laboratory Chemicals-FUJIFILM Wako Chemicals U.S.A. Corporation
![Ligands with 1,10-phenanthroline scaffold for highly regioselective iron-catalyzed alkene hydrosilylation | Nature Communications Ligands with 1,10-phenanthroline scaffold for highly regioselective iron-catalyzed alkene hydrosilylation | Nature Communications](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs41467-017-02472-6/MediaObjects/41467_2017_2472_Fig1_HTML.jpg)