![KR20140107357A - Process for the manufacture of 1-[2-(2,4-dimethyl-phenylsulfanyl)-phenyl]-piperazine - Google Patents](https://patentimages.storage.googleapis.com/6d/7d/2b/150851a9b62c98/pct00014.png "KR20140107357A - Process for the manufacture of 1-[2-(2,4-dimethyl-phenylsulfanyl)-phenyl]-piperazine - Google Patents")
KR20140107357A - Process for the manufacture of 1-[2-(2,4-dimethyl-phenylsulfanyl)-phenyl]-piperazine - Google Patents
Piperazine‐ and DABCO‐bridged dinuclear N‐heterocyclic carbene palladium complexes: synthesis, structure and application to Hiyama coupling reaction - Wang - 2017 - Applied Organometallic Chemistry - Wiley Online Library
Kinetics and mechanism of the substitution behaviour of Pd(ii) piperazine complexes with different biologically relevant nucleophiles - Dalton Transactions (RSC Publishing)
Scheme for synthesis of the piperazine-based SB ligand and its... | Download Scientific Diagram
PDF) Modification of silica using piperazine for immobilization of palladium nanoparticles: A study of its catalytic activity as an efficient heterogeneous catalyst for Heck and Suzuki reactions
DABCO bond cleavage for the synthesis of piperazine derivatives - RSC Advances (RSC Publishing)
Dichloromethane;diphenylphosphanylmethyl(diphenyl)phosphane;ethoxyethane; palladium(2+);piperazine-1,4-dicarbodithioate;ruthenium(2+);triphenylphosphane;ditetrafluoroborate | C99H98B2Cl6F8N2OP6PdRuS4 - PubChem
Palladium supported on modified magnetic nanoparticles: a phosphine‐free and heterogeneous catalyst for Suzuki and Stille reactions - Ghorbani‐Choghamarani - 2016 - Applied Organometallic Chemistry - Wiley Online Library
High Catalytic Activity of Pd Nanoparticles Synthesized from Green Alga Chlorella vulgaris in Buchwald-hartwig Synthesis of N-Aryl Piperazines | Bentham Science
Kinetics of base hydrolysis of α-amino acid esters catalyzed by palladium(II) piperazine complex in: Open Chemistry Volume 8 Issue 4 (2010)
Palladium-Catalyzed Modular Synthesis of Substituted Piperazines and Related Nitrogen Heterocycles. - PDF Download Free
![Process for the manufacture of 1-[2-(2,4-dimethyl-phenylsulfanyl)-phenyl]- piperazine - US 9,133,144 B2 - PatentSwarm](https://images.patentswarm.com/US9133144B2/original.7dd03700e6417622b5fb895e4aadb5de01d668fd706513d0d93dc7980a5585dd.png "Process for the manufacture of 1-[2-(2,4-dimethyl-phenylsulfanyl)-phenyl]- piperazine - US 9,133,144 B2 - PatentSwarm")
Process for the manufacture of 1-[2-(2,4-dimethyl-phenylsulfanyl)-phenyl]- piperazine - US 9,133,144 B2 - PatentSwarm
Pd Catalyzed N1/N4 Arylation of Piperazine for Synthesis of Drugs, Biological and Pharmaceutical Targets: An Overview of Buchwald Hartwig Amination Reaction of Piperazine in Drug Synthesis | Bentham Science
Piperazine synthesis
Applications of Palladium-Catalyzed C–N Cross-Coupling Reactions
EP3141543A1 - New vortioxetine intermediate and synthesis process thereof - Google Patents
Pd-Catalyzed Synthesis of Piperazine Scaffolds Under Aerobic and Solvent-Free Conditions. - Abstract - Europe PMC
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Synthesis of 4-[2-Amino-5-(l-pyrrolidinyl)phenyl]piperazine
Vortioxetine | 508233-74-7
Synthesis of N-arylpiperazines from aryl halides and piperazine under a palladium tri-tert-butylphosphine catalyst - ScienceDirect
Palladium(ii) induced complete conformational enrichment of the syn isomer of N,N′-bis(4-pyridylformyl)piperazine - RSC Advances (RSC Publishing)
Modification of silica using piperazine for immobilization of palladium nanoparticles: a study of its catalytic activity as an efficient heterogeneous catalyst for Heck and Suzuki reactions | SpringerLink
![A practical chromatography-free synthesis of a 5,6-dihydroimidazolo[1,5-f]pteridine derivative as a polo-like kinase-1 inhibitor - Tetrahedron - X-MOL](https://xpic.x-mol.com/20180817%2F10.1016_j.tet.2018.08.020.jpg "A practical chromatography-free synthesis of a 5,6-dihydroimidazolo[1,5-f]pteridine derivative as a polo-like kinase-1 inhibitor - Tetrahedron - X-MOL")
A practical chromatography-free synthesis of a 5,6-dihydroimidazolo[1,5-f]pteridine derivative as a polo-like kinase-1 inhibitor - Tetrahedron - X-MOL
Recent progress toward the asymmetric synthesis of carbon-substituted piperazine pharmacophores and oxidative related heterocycles - RSC Medicinal Chemistry (RSC Publishing) DOI:10.1039/D0MD00053A
