![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
![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
![Palladium-1,10-phenanthroline complex encaged in Y zeolite: An efficient and highly recyclable heterogeneous catalyst for aminocarbonylation - ScienceDirect Palladium-1,10-phenanthroline complex encaged in Y zeolite: An efficient and highly recyclable heterogeneous catalyst for aminocarbonylation - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0926860X1400012X-fx1.jpg)
Palladium-1,10-phenanthroline complex encaged in Y zeolite: An efficient and highly recyclable heterogeneous catalyst for aminocarbonylation - ScienceDirect
ChemIDplus - 132958-37-3 - QSAYSJLDPMTKTP-UHFFFAOYSA-L - 1,10-Phenanthroline-glycine palladium(II) - Similar structures search, synonyms, formulas, resource links, and other chemical information.
Direct arylation of phenanthroline derivatives via oxidative C–H/C–H cross-coupling: synthesis and discovery of excellent ligands - Organic & Biomolecular Chemistry (RSC Publishing)
![The palladium–phenanthroline catalyzed carbonylation of nitroarenes to diarylureas: Effect of chloride and diphenylphosphinic acid - ScienceDirect The palladium–phenanthroline catalyzed carbonylation of nitroarenes to diarylureas: Effect of chloride and diphenylphosphinic acid - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0022328X05002986-fx1.gif)
The palladium–phenanthroline catalyzed carbonylation of nitroarenes to diarylureas: Effect of chloride and diphenylphosphinic acid - ScienceDirect
![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.png)
Scheme 1 Synthesis of phenanthroline-and Pd(II)-phenanthroline-based... | Download Scientific Diagram
![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-gr5.jpg)
Design and synthesis of chiral 1,10-phenanthroline ligand, and application in palladium catalyzed asymmetric 1,4-addition reactions - 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
![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
![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)