Practical synthesis of polysubstituted unsymmetric 1,10-phenanthrolines by palladium catalyzed intramolecular oxidative cross coupling of C(sp2)–H and C(sp3)–H bonds of carboxamides - Organic Chemistry Frontiers (RSC Publishing)
![Acetato(2,9-dimethyl-1,10-phenanthroline)palladium(II) dimer bis(trifluoromethanesulfonate), 99% CAS#: 959698-19-2 Acetato(2,9-dimethyl-1,10-phenanthroline)palladium(II) dimer bis(trifluoromethanesulfonate), 99% CAS#: 959698-19-2](http://www.chemicalbook.com/NewsImg/2018-04-12/20184121418558414.jpg)
Acetato(2,9-dimethyl-1,10-phenanthroline)palladium(II) dimer bis(trifluoromethanesulfonate), 99% CAS#: 959698-19-2
![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/43f34j00lHcUIPbBbokq/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
![Crystal structure of diiodo(1,10-phenanthroline-κ2N,N′)palladium(II), PdI2(C12H8N2) : Zeitschrift für Kristallographie - New Crystal Structures Crystal structure of diiodo(1,10-phenanthroline-κ2N,N′)palladium(II), PdI2(C12H8N2) : Zeitschrift für Kristallographie - New Crystal Structures](https://www.degruyter.com/view/j/ncrs.2010.225.issue-2/ncrs.2010.0138/ncrs.2010.0138.png)
Crystal structure of diiodo(1,10-phenanthroline-κ2N,N′)palladium(II), PdI2(C12H8N2) : Zeitschrift für Kristallographie - New Crystal Structures
![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
![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
![PDF) Friedel–Crafts-Type Alkylation of Indoles in Water Using Amphiphilic Resin-Supported 1,10-Phenanthroline–Palladium Complex under Aerobic Conditions PDF) Friedel–Crafts-Type Alkylation of Indoles in Water Using Amphiphilic Resin-Supported 1,10-Phenanthroline–Palladium Complex under Aerobic Conditions](https://www.researchgate.net/publication/339071503/figure/tbl2/AS:855561587417089@1580993186731/Friedel-Crafts-type-alkylation-of-indoles-2-with-allyl-esters-3-in-H2O_Q320.jpg)
PDF) Friedel–Crafts-Type Alkylation of Indoles in Water Using Amphiphilic Resin-Supported 1,10-Phenanthroline–Palladium Complex under Aerobic Conditions
![Design of bifunctional chiral phenanthroline ligand with Lewis basic site for palladium-catalyzed asymmetric allylic substitution - Chemical Communications (RSC Publishing) DOI:10.1039/C8CC00754C Design of bifunctional chiral phenanthroline ligand with Lewis basic site for palladium-catalyzed asymmetric allylic substitution - Chemical Communications (RSC Publishing) DOI:10.1039/C8CC00754C](https://pubs.rsc.org/image/article/2018/CC/c8cc00754c/c8cc00754c-f2_hi-res.gif)
Design of bifunctional chiral phenanthroline ligand with Lewis basic site for palladium-catalyzed asymmetric allylic substitution - Chemical Communications (RSC Publishing) DOI:10.1039/C8CC00754C
![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
1,10-Phenanthroline, 2,9-dimethyl-4,7-diphenyl-, palladium salt, acetate (1:1:2) | C30H28N2O4Pd | ChemSpider
![Scheme 1 Synthesis of phenanthroline-and Pd(II)-phenanthroline-based... | Download Scientific Diagram Scheme 1 Synthesis of phenanthroline-and Pd(II)-phenanthroline-based... | Download Scientific Diagram](https://www.researchgate.net/publication/331725014/figure/fig1/AS:743659255390208@1554313591571/Scheme-1-Synthesis-of-phenanthroline-and-PdII-phenanthroline-based-microporous-organic_Q320.jpg)