![Synthesis of Benzimidazole‐Fused Medium‐Sized N,S‐Heterocycles via Palladium‐Catalyzed Cyclizations,European Journal of Organic Chemistry - X-MOL Synthesis of Benzimidazole‐Fused Medium‐Sized N,S‐Heterocycles via Palladium‐Catalyzed Cyclizations,European Journal of Organic Chemistry - X-MOL](https://xpic.x-mol.com/20190107%2F10.1002_ejoc.201801686.jpg)
Synthesis of Benzimidazole‐Fused Medium‐Sized N,S‐Heterocycles via Palladium‐Catalyzed Cyclizations,European Journal of Organic Chemistry - X-MOL
![Arylation of heterocyclic compounds by benzimidazole-based N-heterocyclic carbene-palladium(II) complexes - ScienceDirect Arylation of heterocyclic compounds by benzimidazole-based N-heterocyclic carbene-palladium(II) complexes - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0022328X19305194-gr1.jpg)
Arylation of heterocyclic compounds by benzimidazole-based N-heterocyclic carbene-palladium(II) complexes - ScienceDirect
![Enhanced separation of Pd(II) and Pt(IV) from hydrochloric acid aqueous solution using 2-((2-methoxyethyl)thio)-1H-benzimidazole | SpringerLink Enhanced separation of Pd(II) and Pt(IV) from hydrochloric acid aqueous solution using 2-((2-methoxyethyl)thio)-1H-benzimidazole | SpringerLink](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs12598-020-01545-8/MediaObjects/12598_2020_1545_Figa_HTML.png)
Enhanced separation of Pd(II) and Pt(IV) from hydrochloric acid aqueous solution using 2-((2-methoxyethyl)thio)-1H-benzimidazole | SpringerLink
Heck reaction using palladium-benzimidazole catalyst: synthesis, characterisation and catalytic activity
![Metal-free selective synthesis of 2-substituted benzimidazoles catalyzed by Brönsted acidic ionic liquid: Convenient access to one-pot synthesis of N-alkylated 1,2-disubstituted benzimidazoles - Tetrahedron - X-MOL Metal-free selective synthesis of 2-substituted benzimidazoles catalyzed by Brönsted acidic ionic liquid: Convenient access to one-pot synthesis of N-alkylated 1,2-disubstituted benzimidazoles - Tetrahedron - X-MOL](https://xpic.x-mol.com/20190517%2F10.1016_j.tet.2019.05.014.jpg)
Metal-free selective synthesis of 2-substituted benzimidazoles catalyzed by Brönsted acidic ionic liquid: Convenient access to one-pot synthesis of N-alkylated 1,2-disubstituted benzimidazoles - Tetrahedron - X-MOL
![Arylation of heterocyclic compounds by benzimidazole-based N-heterocyclic carbene-palladium(II) complexes - ScienceDirect Arylation of heterocyclic compounds by benzimidazole-based N-heterocyclic carbene-palladium(II) complexes - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0022328X19305194-fx1.jpg)
Arylation of heterocyclic compounds by benzimidazole-based N-heterocyclic carbene-palladium(II) complexes - ScienceDirect
![Sequential Metal‐Catalyzed N‐Heteroarylation and C–C Cross‐Coupling Reactions: An Expedient Route to Tris(hetero)aryl Systems - Siddle - 2008 - European Journal of Organic Chemistry - Wiley Online Library Sequential Metal‐Catalyzed N‐Heteroarylation and C–C Cross‐Coupling Reactions: An Expedient Route to Tris(hetero)aryl Systems - Siddle - 2008 - European Journal of Organic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/052a0217-6cd3-4832-a4c2-3098ee3eb2ab/mfig000.jpg)
Sequential Metal‐Catalyzed N‐Heteroarylation and C–C Cross‐Coupling Reactions: An Expedient Route to Tris(hetero)aryl Systems - Siddle - 2008 - European Journal of Organic Chemistry - Wiley Online Library
![PDF) An Efficient Synthesis of Benzimidazoles via Palladium-Catalyzed Amine Exchange Reaction from Trialkylamines to o-Phenylenediamine in an Aqueous Medium PDF) An Efficient Synthesis of Benzimidazoles via Palladium-Catalyzed Amine Exchange Reaction from Trialkylamines to o-Phenylenediamine in an Aqueous Medium](https://www.researchgate.net/profile/Chan_Cho/publication/263634689/figure/tbl1/AS:669005534736392@1536514757412/Pd-C-catalyzed-synthesis-of-benzimidazoles-from-1-and-2_Q320.jpg)
PDF) An Efficient Synthesis of Benzimidazoles via Palladium-Catalyzed Amine Exchange Reaction from Trialkylamines to o-Phenylenediamine in an Aqueous Medium
![Scheme 1 | Catalytic activity of a supported palladium–benzimidazole complex toward alkene hydrogenation | SpringerLink Scheme 1 | Catalytic activity of a supported palladium–benzimidazole complex toward alkene hydrogenation | SpringerLink](https://media.springernature.com/full/springer-static/image/art%3A10.1007%2Fs11243-012-9597-0/MediaObjects/11243_2012_9597_Sch1_HTML.gif)
Scheme 1 | Catalytic activity of a supported palladium–benzimidazole complex toward alkene hydrogenation | SpringerLink
![Ionically tagged benzimidazole palladium(II) complex: preparation and catalytic application in cross-coupling reactions - ScienceDirect Ionically tagged benzimidazole palladium(II) complex: preparation and catalytic application in cross-coupling reactions - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0040403911008288-fx1.jpg)
Ionically tagged benzimidazole palladium(II) complex: preparation and catalytic application in cross-coupling reactions - ScienceDirect
![Palladium -catalyzed aerobic oxidative C–H amination: synthesis of 2-unsubstituted and 2-substituted N -aryl benzimidazoles - RSC Advances (RSC Publishing) DOI:10.1039/C2RA20328F Palladium -catalyzed aerobic oxidative C–H amination: synthesis of 2-unsubstituted and 2-substituted N -aryl benzimidazoles - RSC Advances (RSC Publishing) DOI:10.1039/C2RA20328F](https://pubs.rsc.org/image/article/2012/RA/c2ra20328f/c2ra20328f-s1.gif)
Palladium -catalyzed aerobic oxidative C–H amination: synthesis of 2-unsubstituted and 2-substituted N -aryl benzimidazoles - RSC Advances (RSC Publishing) DOI:10.1039/C2RA20328F
![Benzimidazole bearing Pd–PEPPSI complexes catalyzed direct C2‐arylation/heteroarylation of N‐substituted benzimidazoles - Gokanapalli - 2020 - Applied Organometallic Chemistry - Wiley Online Library Benzimidazole bearing Pd–PEPPSI complexes catalyzed direct C2‐arylation/heteroarylation of N‐substituted benzimidazoles - Gokanapalli - 2020 - Applied Organometallic Chemistry - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/8b6d83ac-4479-477c-9b35-f4233ec5da7a/aoc5869-toc-0001-m.jpg)
Benzimidazole bearing Pd–PEPPSI complexes catalyzed direct C2‐arylation/heteroarylation of N‐substituted benzimidazoles - Gokanapalli - 2020 - Applied Organometallic Chemistry - Wiley Online Library
![Catalysts | Free Full-Text | Microwave-Assisted Palladium-Catalyzed Cross-Coupling Reactions: Generation of Carbon–Carbon Bond | HTML Catalysts | Free Full-Text | Microwave-Assisted Palladium-Catalyzed Cross-Coupling Reactions: Generation of Carbon–Carbon Bond | HTML](https://www.mdpi.com/catalysts/catalysts-10-00004/article_deploy/html/images/catalysts-10-00004-sch011.png)
Catalysts | Free Full-Text | Microwave-Assisted Palladium-Catalyzed Cross-Coupling Reactions: Generation of Carbon–Carbon Bond | HTML
![Arylation of heterocyclic compounds by benzimidazole-based N-heterocyclic carbene-palladium(II) complexes - ScienceDirect Arylation of heterocyclic compounds by benzimidazole-based N-heterocyclic carbene-palladium(II) complexes - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0022328X19305194-sc2.jpg)
Arylation of heterocyclic compounds by benzimidazole-based N-heterocyclic carbene-palladium(II) complexes - ScienceDirect
![PDF) Heck reaction using palladium-benzimidazole catalyst: synthesis, characterisation and catalytic activity PDF) Heck reaction using palladium-benzimidazole catalyst: synthesis, characterisation and catalytic activity](https://i1.rgstatic.net/publication/329895405_Heck_reaction_using_palladium-benzimidazole_catalyst_synthesis_characterisation_and_catalytic_activity/links/5c2115d492851c22a3443194/largepreview.png)
PDF) Heck reaction using palladium-benzimidazole catalyst: synthesis, characterisation and catalytic activity
![Formation of polynuclear palladium complexes with the benzimidazole-2-thiolate anion | Semantic Scholar Formation of polynuclear palladium complexes with the benzimidazole-2-thiolate anion | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/cc5409ed59d35caf79f989d13cdc985e2681c640/2-Figure1-1.png)
Formation of polynuclear palladium complexes with the benzimidazole-2-thiolate anion | Semantic Scholar
![PDF) Palladium-Catalyzed Aryl C H Activation and Tandem ortho- Hydroxylation/Alkoxylation of 2-Aryl Benzimidazoles: Cytotoxicity and DNA-Binding Studies | Satish Manda - Academia.edu PDF) Palladium-Catalyzed Aryl C H Activation and Tandem ortho- Hydroxylation/Alkoxylation of 2-Aryl Benzimidazoles: Cytotoxicity and DNA-Binding Studies | Satish Manda - Academia.edu](https://0.academia-photos.com/attachment_thumbnails/39779136/mini_magick20190222-29796-vqufn5.png?1550855115)
PDF) Palladium-Catalyzed Aryl C H Activation and Tandem ortho- Hydroxylation/Alkoxylation of 2-Aryl Benzimidazoles: Cytotoxicity and DNA-Binding Studies | Satish Manda - Academia.edu
![PDF] catena-Poly[[bis(1H-benzimidazole-κN 3)palladium(II)]-μ-benzene-1,4-dicarboxylato-κ2 O 1:O 4] | Semantic Scholar PDF] catena-Poly[[bis(1H-benzimidazole-κN 3)palladium(II)]-μ-benzene-1,4-dicarboxylato-κ2 O 1:O 4] | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/08fac28127f1e880caa63d6e1acc0cab376947a4/1-Table2-1.png)
PDF] catena-Poly[[bis(1H-benzimidazole-κN 3)palladium(II)]-μ-benzene-1,4-dicarboxylato-κ2 O 1:O 4] | Semantic Scholar
1-Methyl-3-[1-[2-(3-methylbenzimidazol-1-yl)naphthalen-1-yl]naphthalen-2-yl] benzimidazole;palladium(2+);2,2,2-trifluoroacetate | C40H26F6N4O4Pd - PubChem
![PDF) 5-Nitrobenzimidazole containing Pd(II) catalyzed C-C cross-coupling reactions: The effect of the N-substituent of the benzimidazole structure on catalyst activity PDF) 5-Nitrobenzimidazole containing Pd(II) catalyzed C-C cross-coupling reactions: The effect of the N-substituent of the benzimidazole structure on catalyst activity](https://www.researchgate.net/profile/Kenan_Buldurun/publication/332745277/figure/fig1/AS:756753960534016@1557435612088/Scheme-1-Synthesis-of-palladium-N-5-nitrobenzimidazole-complexes_Q320.jpg)
PDF) 5-Nitrobenzimidazole containing Pd(II) catalyzed C-C cross-coupling reactions: The effect of the N-substituent of the benzimidazole structure on catalyst activity
![Synthesis, crystal structures and biological activities of palladium(II) complexes of benzimidazole and 2-methylbenzimidazole - ScienceDirect Synthesis, crystal structures and biological activities of palladium(II) complexes of benzimidazole and 2-methylbenzimidazole - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S027753871930436X-ga1.jpg)
Synthesis, crystal structures and biological activities of palladium(II) complexes of benzimidazole and 2-methylbenzimidazole - ScienceDirect
![Table 1 from Substituted 2-(2''-pyridyl)benzimidazole palladium(II) complexes as an efficient catalytic system for Suzuki--Miyaura cross-coupling reactions | Semantic Scholar Table 1 from Substituted 2-(2''-pyridyl)benzimidazole palladium(II) complexes as an efficient catalytic system for Suzuki--Miyaura cross-coupling reactions | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/a8a05024b5eea15888eb6370f0714193ebb80e55/5-Table2-1.png)
Table 1 from Substituted 2-(2''-pyridyl)benzimidazole palladium(II) complexes as an efficient catalytic system for Suzuki--Miyaura cross-coupling reactions | Semantic Scholar
![Palladium(ii) ligated with a selenated (Se, CNHC, N-)-type pincer ligand: an efficient catalyst for Mizoroki-Heck and Suzuki-Miyaura coupling in water. - Org. Biomol. Chem. - X-MOL Palladium(ii) ligated with a selenated (Se, CNHC, N-)-type pincer ligand: an efficient catalyst for Mizoroki-Heck and Suzuki-Miyaura coupling in water. - Org. Biomol. Chem. - X-MOL](https://xpic.x-mol.com/20191102%2F10.1039_C9OB01674K.jpg)
Palladium(ii) ligated with a selenated (Se, CNHC, N-)-type pincer ligand: an efficient catalyst for Mizoroki-Heck and Suzuki-Miyaura coupling in water. - Org. Biomol. Chem. - X-MOL
![Synthesis and structural characterization of 20-membered macrocyclic rings bearing trans -chelating bis(N-heterocyclic carbene) ligands and the cataly ... - Dalton Transactions (RSC Publishing) DOI:10.1039/C9DT02147G Synthesis and structural characterization of 20-membered macrocyclic rings bearing trans -chelating bis(N-heterocyclic carbene) ligands and the cataly ... - Dalton Transactions (RSC Publishing) DOI:10.1039/C9DT02147G](https://pubs.rsc.org/image/article/2019/DT/c9dt02147g/c9dt02147g-s4_hi-res.gif)
Synthesis and structural characterization of 20-membered macrocyclic rings bearing trans -chelating bis(N-heterocyclic carbene) ligands and the cataly ... - Dalton Transactions (RSC Publishing) DOI:10.1039/C9DT02147G
![PDF) Heck reaction using palladium-benzimidazole catalyst: synthesis, characterisation and catalytic activity PDF) Heck reaction using palladium-benzimidazole catalyst: synthesis, characterisation and catalytic activity](https://www.researchgate.net/publication/329895405/figure/fig2/AS:707414437404673@1545672153471/Synthesis-route-of-palladium-catalyst-where-R-H-or-Cl_Q320.jpg)
PDF) Heck reaction using palladium-benzimidazole catalyst: synthesis, characterisation and catalytic activity
![P,N]-phosphinobenzimidazole ligands in palladium-catalyzed C-N cross-coupling reactions: The effect of the N-substituent of the benzimidazole scaffold on catalyst performance - ScienceDirect P,N]-phosphinobenzimidazole ligands in palladium-catalyzed C-N cross-coupling reactions: The effect of the N-substituent of the benzimidazole scaffold on catalyst performance - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0022328X17302395-fx1.jpg)
P,N]-phosphinobenzimidazole ligands in palladium-catalyzed C-N cross-coupling reactions: The effect of the N-substituent of the benzimidazole scaffold on catalyst performance - ScienceDirect
![A Novel Conjugated Polymer Consists of Benzimidazole and Benzothiadiazole: Synthesis, Photophysics Properties, and Sensing Properties for Pd2+ - J. Polym. Sci. A Polym. Chem. - X-MOL A Novel Conjugated Polymer Consists of Benzimidazole and Benzothiadiazole: Synthesis, Photophysics Properties, and Sensing Properties for Pd2+ - J. Polym. Sci. A Polym. Chem. - X-MOL](https://xpic.x-mol.com/20200121%2F10.1002_pol.20200005.jpg)