Magnetic Ru catalyst in Heck, Suzuki, and Sonagashira C–C coupling reactions
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OpenAlex topics: Catalytic Cross-Coupling Reactions · Chemical Synthesis and Analysis · Innovative Microfluidic and Catalytic Techniques Innovation
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References (41)
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1. Suzuki N, Koyama S, Koike R, Ebara N, Arai R, Takeoka Y, Rikukawa M, Tsai FY (2021) Palladium-catalyzed Mizoroki-Heck and copper-free Sonogashira coupling reactions in water using thermoresponsive polymer micelles. Polymers. https://doi.org/10.3390/polym1316271710.3390/polym13162717 ↗
2. Ghasemi S, Karim S (2017) Mizoroki-Heck cross-coupling reaction of haloarenes mediated by a well-controlled modified polyacrylamide brush grafted silica/pd nanoparticle system. BCSJ. https://doi.org/10.1246/bcsj.2016037410.1246/bcsj.20160374 ↗
3. Zhao F, Tan B, Li Q, Tan Q, Huang H (2022) Progress in C-C and C-heteroatom bonds construction using alcohols as acyl precursors. Molecules. https://doi.org/10.3390/molecules2724897710.3390/molecules27248977 ↗
4. Chemler SR, Trauner D, Danishefsky SJ (2001) The B-alkyl Suzuki-Miyaura cross-coupling reaction: development, mechanistic study, and applications in natural product synthesis. Angew Chem Int Ed Engl. https://doi.org/10.1002/1521-3773(20011217)40:24/3C4544::aid-anie4544/3E3.0.co;2-N10.1002/1521-3773(20011217)40:24/3C4544::aid-anie4544/3E3.0.co;2-N ↗
5. Dhakshinamoorthy A, Asiri AM, Garcia H (2018) Formation of C-C and C–heteroatom bonds by C–H activation by metal organic frameworks as catalysts or supports. ACS Catal. https://doi.org/10.1021/acscatal.8b0450610.1021/acscatal.8b04506 ↗
6. Yasukawa T, Miyamuraa H, Kobayashi S (2014) Chiral metal nanoparticle-catalyzed asymmetric C-C bond formation reactions. Chem Soc Rev. https://doi.org/10.1039/c3cs60298b10.1039/c3cs60298b ↗
7. Kamigata N, Ozaki J, Kobayashi M (1985) Reaction of alkenesulfonyl chlorides with olefins catalyzed by a ruthenium (II) complex. A novel method for synthesis of (E,E)-1,4-diaryl1,3-butadienes. J Org Chem. https://doi.org/10.1021/jo00225a00910.1021/jo00225a009 ↗
8. Imazaki Y, Shirakawa E, Ueno R, Hayashi T (2012) Ruthenium-catalyzed transformation of aryl and alkenyl triflates to halides. J Am Chem Soc. https://doi.org/10.1021/ja307771d10.1021/ja307771d ↗
9. Mitsudo T, Takagi M, Zhang SW, Watanabe Y (1992) Ruthenium complex-catalyzed coupling of vinyl halides with olefins. J Organomet Chem. https://doi.org/10.1016/0022-328X(92)83134-410.1016/0022-328X(92)83134-4 ↗
10. Littke AF, Fu GC (2002) Palladium-catalyzed coupling reactions of aryl chlorides. Angew Chem Int Ed. https://doi.org/10.1002/1521-3773(20021115)41:22/3C4176::AID-ANIE4176/3E3.0.CO;2-U10.1002/1521-3773(20021115)41:22/3C4176::AID-ANIE4176/3E3.0.CO;2-U ↗
11. Ackermann L, Born R, Bercedo PA (2007) Ruthenium (IV) alkylidenes as pre-catalysts for direct arylations of alkenes with aryl chlorides and an application to sequential catalysis. Angew Chem Int Ed. https://doi.org/10.1002/anie.20070172710.1002/anie.200701727 ↗
12. Littke AF, Fu GC (2001) A versatile catalyst for Heck reactions of aryl chlorides and aryl bromides under mild conditions. J Am Chem Soc. https://doi.org/10.1021/ja010988c10.1021/ja010988c ↗
13. Salam N, Kundu SK, Roy AS, Mondal P, Ghosh K, Bhaumik A, Islam SM (2014) A ruthenium-grafted triazine functionalized mesoporous polymer: a highly efficient and multifunctional catalyst for transfer hydrogenation and the Suzuki-Miyaura cross-coupling reactions. Dalton Trans. https://doi.org/10.1039/C3DT53158A10.1039/C3DT53158A ↗
14. Mohammadinejad R, Karimi S, Iravani S, Varma RS (2016) Plant-derived nanostructures: types and applications. Green Chem. https://doi.org/10.1039/C5GC01403D10.1039/C5GC01403D ↗
15. Srivastava V (2023) Continuous-flow synthesis of ruthenium nanoparticles using a microreactor for the selective hydrogenation reaction. Lett Org Chem. https://doi.org/10.2174/157017862066623060611024310.2174/1570178620666230606110243 ↗
16. Magerlein W, Dreisbach C, Hugl H, Tse MK, Klawonn M, Bhor S, Beller M (2007) Homogeneous and heterogeneous ruthenium catalysts in the synthesis of fine chemicals. Catal Today. https://doi.org/10.1016/j.cattod.2006.11.02410.1016/j.cattod.2006.11.024 ↗
17. Feng Z, Liu X, Wang Y, Meng C (2021) Recent advances on gallium-modified ZSM-5 for conversion of light hydrocarbons. Molecules. https://doi.org/10.3390/molecules2608223410.3390/molecules26082234 ↗
18. Chancellor AJ, Seymour BT, Zhao B (2019) Characterizing polymer-grafted nanoparticles: from basic defining parameters to behavior in solvents and self-assembled structures. Anal Chem. https://doi.org/10.1021/acs.analchem.9b0070710.1021/acs.analchem.9b00707 ↗
19. Chen Y, Renner P, Liang H (2019) Dispersion of nanoparticles in lubricating oil: a critical review. Lubricants. https://doi.org/10.3390/lubricants701000710.3390/lubricants7010007 ↗
20. Gu H, Xu K, Xu C, Huang J (2006) Biofunctional magnetic nanoparticles for protein separation and pathogen detection. Chem Commun. https://doi.org/10.1039/B514130C10.1039/B514130C ↗
21. Lu Q, Choi K, Nam JD, Choi HJ (2021) Magnetic polymer composite particles: design and magnetorheology. Polymers. https://doi.org/10.3390/polym1304051210.3390/polym13040512 ↗
22. Banan A, Bayat A, Valizadeh H (2017) Copper immobilized onto polymer-coated magnetic nanoparticles as recoverable catalyst for ‘click’ reaction. Appl Organomet Chem. https://doi.org/10.1002/aoc.360410.1002/aoc.3604 ↗
23. Zhu L, Liu XQ, Jiang HL, Sun LB (2017) Metal-organic frameworks for heterogeneous basic catalysis. Chem Rev. https://doi.org/10.1021/acs.chemrev.7b0009110.1021/acs.chemrev.7b00091 ↗
24. Park S, Kim M, Koo DH, Chang S (2004) Use of ruthenium/alumina as a convenient catalyst for copper-free Sonogashira coupling reactions. Adv Synth Catal. https://doi.org/10.1002/adsc.20040418910.1002/adsc.200404189 ↗
25. Ghasemi S, Ahmadi L, Farjadian F (2022) Thermo-responsive PNIPAAm-b-PLA amphiphilic block copolymer micelle as nanoplatform for docetaxel drug release. J Mater Sci. https://doi.org/10.1007/s10853-022-07711-w10.1007/s10853-022-07711-w ↗
26. Ghasemi S, Harandi ZA (2019) PdNPs@ thermo-responsive block copolymers composed of PNIPAM and poly (ionic liquid) via RAFT polymerization. Polym Bull. https://doi.org/10.1007/s00289-018-2532-610.1007/s00289-018-2532-6 ↗
27. Ghasemi S, Farjadian F, Tamami B (2016) Biaryl formation via Suzuki and Stille coupling reactions using palladium nanoparticle/polymeric N-heterocyclic carbene grafted silica as recyclable and efficient catalyst. Appl Organomet Chem. https://doi.org/10.1002/aoc.350810.1002/aoc.3508 ↗
28. Tamami B, Farjadian F, Ghasemi S, Allahyari H, Mirzadeh M (2015) Palladium nanoparticles supported on poly(n-vinylpyrrolidone)-grafted silica as an efficient catalyst for copper-free Sonogashira and Suzuki cross-coupling. J Braz Chem Soc 26:1591–1598. https://doi.org/10.5935/0103-5053.2015012910.5935/0103-5053.20150129 ↗
29. Tamami B, Allahyari H, Farjadian F, Ghasemi S (2011) Synthesis and applications of poly (N-vinylimidazole) grafted silica-containing palladium nanoparticles as a new re-cyclable catalyst for Heck, Sonogashira and Suzuki coupling. Iran Polym J. https://sid.ir/paper/574904/en
30. Farjadian F, Tamami B (2014) Poly(vinylpyridine)-grafted silica containing palladium or nickel nanoparticles as heterogeneous catalysts for the Sonogashira coupling reaction. ChemPlusChem. https://doi.org/10.1002/cplu.20140216910.1002/cplu.201402169 ↗
31. Tamami B, Dodeji FN, Ghasemi S (2015) Palladium nanoparticles supported on modified polystyrene resin as a polymeric catalyst for Sonogashira-Hagihara coupling reactions. Turk J Chem. https://doi.org/10.3906/kim-1407-2210.3906/kim-1407-22 ↗
32. Kafshboran HR, Ghasemi S (2023) Au nanoparticles decorated on EDTA functionalized Poly (NIPAM-co-allylamine) grafted Fe3O4 for reduction of nitroarenes. Mater Chem Phys. https://doi.org/10.1016/j.matchemphys.2023.12823710.1016/j.matchemphys.2023.128237 ↗
33. Kafshboran HR, Ghasemi S (2024) Designing magnetic catalysts based on gold nanoparticles supported by ethylenediamine tetraacetic acid functionalized amino-modified poly (N-isopropyl acrylamide) for reduction of nitro compounds in water. Polym Int. https://doi.org/10.1002/pi.662510.1002/pi.6625 ↗
34. Xu J, Ju C, Sheng J, Wang F, Zhang Q, Sun G, Sun M (2013) Synthesis and characterization of magnetic nanoparticles and its application in lipase immobilization. Bull Korean Chem Soc. https://doi.org/10.5012/bkcs.2013.34.8.240810.5012/bkcs.2013.34.8.2408 ↗
35. Tee SY, Lee CJJ, Dinachali SS, Lai SC, Williams EL, Luo HK, Chi D, Hor TSA, Han MY (2015) Amorphous ruthenium nanoparticles for enhanced electrochemical water splitting. Nanotechnol. https://doi.org/10.1088/0957-4484/26/41/41540110.1088/0957-4484/26/41/415401 ↗
36. Pollini I (1994) Photoemission study of the electronic structure of CrC13 and RuC13 compounds. Phys Rev B. https://doi.org/10.1103/PhysRevB.50.209510.1103/PhysRevB.50.2095 ↗
37. Lee YY, Parker SG, Barfidokht A, Alam MT, Walker DB, Messerle BA, Gooding JJ (2015) A ruthenium based organometallic complex for biosensing that is both a stable redox label and a homobifunctional linker. Electroanalysis. https://doi.org/10.1002/elan.20140064210.1002/elan.201400642 ↗
38. Murata S, Aika K (1992) Preparation and characterization of chlorine-free ruthenium catalysts and the promoter effect in ammonia synthesis: a lanthanide oxide-promoted Ru/Al2O3 catalyst. J Catal. https://doi.org/10.1016/0021-9517(92)90111-T10.1016/0021-9517(92)90111-T ↗
39. Prasad S, Rodene DD, Burkholder MB, Donald KJ, Gupton BF (2021) Substituent effects and the energetics of noncatalyzed aryl halide aminations: a theoretical investigation. ACS Omega. https://doi.org/10.1021/acsomega.1c0393410.1021/acsomega.1c03934 ↗
40. Wang H, Li X, Ruan Q, Tang J (2020) Ru and RuOx decorated carbon nitride for efficient ammonia photosynthesis. Nanoscale. https://doi.org/10.1039/D0NR02527E10.1039/D0NR02527E ↗
41. Akbari S, Mokhtari J, Mirjafari Z (2017) Solvent-free and melt aerobic oxidation of benzyl alcohols using Pd/Cu2(BDC)2DABCO–MOF prepared by one-step and through reduction by dimethylformamide. RSC Adv. https://doi.org/10.1039/C7RA07209K10.1039/C7RA07209K ↗