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Palladium(ii) ligated with a selenated (Se, CNHC, N-)-type pincer ligand: an efficient catalyst for Mizoroki-Heck and Suzuki-Miyaura coupling in water.,Organic & Biomolecular Chemistry - X-MOL
Heck reaction using palladium-benzimidazole catalyst: synthesis, characterisation and catalytic activity
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Enhanced separation of Pd(II) and Pt(IV) from hydrochloric acid aqueous solution using 2-((2-methoxyethyl)thio)-1H-benzimidazole | SpringerLink
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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
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PDF) Heck reaction using palladium-benzimidazole catalyst: synthesis, characterisation and catalytic activity
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Table 2 from Substituted 2-(2''-pyridyl)benzimidazole palladium(II) complexes as an efficient catalytic system for Suzuki--Miyaura cross-coupling reactions | Semantic Scholar
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Scheme 1 | Catalytic activity of a supported palladium–benzimidazole complex toward alkene hydrogenation | SpringerLink
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A Palladium‐Catalyzed Regiospecific Synthesis of N‐Aryl Benzimidazoles - Zheng - 2007 - Angewandte Chemie - Wiley Online Library
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Arylation of heterocyclic compounds by benzimidazole-based N-heterocyclic carbene-palladium(II) complexes - ScienceDirect
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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
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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
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Pyridyl)benzoazole palladium(ii) complexes as homogeneous catalysts in hydrogenation of alkenes and alkynes - Catalysis Science & Technology (RSC Publishing)
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Ionically tagged benzimidazole palladium(II) complex: preparation and catalytic application in cross-coupling reactions - ScienceDirect
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Synthesis of Benzimidazole‐Fused Medium‐Sized N,S‐Heterocycles via Palladium‐Catalyzed Cyclizations,European Journal of Organic Chemistry - X-MOL
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