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For: Martina K, Manzoli M, Gaudino EC, Cravotto G. Eco-Friendly Physical Activation Methods for Suzuki–Miyaura Reactions. Catalysts 2017;7:98. [DOI: 10.3390/catal7040098] [Cited by in Crossref: 26] [Cited by in F6Publishing: 26] [Article Influence: 4.3] [Reference Citation Analysis]
Number Citing Articles
1 Salih KSM. Modern Development in Copper‐ and Nickel‐Catalyzed Cross‐Coupling Reactions: Formation of Carbon‐Carbon and Carbon‐Heteroatom bonds under Microwave Irradiation Conditions. Asian J of Organic Chemis. [DOI: 10.1002/ajoc.202200023] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
2 Bakhtiarian M, Khodaei MM. Sonochemical synthesis of 1,4-dihydropyridines using a bio-derived magnetic nanocomposite based on the pectin modified with the di-sulfonic acids under mild conditions. Materials Today Communications 2021;29:102791. [DOI: 10.1016/j.mtcomm.2021.102791] [Reference Citation Analysis]
3 Akkoç S. Importance of some factors on the Suzuki‐Miyaura cross‐coupling reaction. J Chin Chem Soc 2021;68:942-51. [DOI: 10.1002/jccs.202000351] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
4 Jose DE, Kanchana US, Mathew TV, Anilkumar G. Recent studies in Suzuki-Miyaura cross-coupling reactions with the aid of phase transfer catalysts. Journal of Organometallic Chemistry 2020;927:121538. [DOI: 10.1016/j.jorganchem.2020.121538] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 4.3] [Reference Citation Analysis]
5 Salih KSM, Baqi Y. Microwave-Assisted Palladium-Catalyzed Cross-Coupling Reactions: Generation of Carbon–Carbon Bond. Catalysts 2020;10:4. [DOI: 10.3390/catal10010004] [Cited by in Crossref: 30] [Cited by in F6Publishing: 30] [Article Influence: 7.5] [Reference Citation Analysis]
6 Yılmaz Baran N. Palladium nanoparticles decorated on a novel polyazomethine as a highly productive and recyclable catalyst for Suzuki coupling reactions and 4-nitrophenol reduction. Journal of Organometallic Chemistry 2019;899:120886. [DOI: 10.1016/j.jorganchem.2019.120886] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 1.5] [Reference Citation Analysis]
7 Baran T. Highly recoverable, reusable, cost-effective, and Schiff base functionalized pectin supported Pd(II) catalyst for microwave-accelerated Suzuki cross-coupling reactions. International Journal of Biological Macromolecules 2019;127:232-9. [DOI: 10.1016/j.ijbiomac.2019.01.046] [Cited by in Crossref: 31] [Cited by in F6Publishing: 33] [Article Influence: 7.8] [Reference Citation Analysis]
8 Varma RS, Len C. Glycerol valorization under continuous flow conditions-recent advances. Current Opinion in Green and Sustainable Chemistry 2019;15:83-90. [DOI: 10.1016/j.cogsc.2018.11.003] [Cited by in Crossref: 46] [Cited by in F6Publishing: 46] [Article Influence: 11.5] [Reference Citation Analysis]
9 Kotha S, Khedkar P, Dommaraju Y. Synthetic applications of rongalite: A green tool in the service of Diels–Alder chemistry and beyond. Tetrahedron Letters 2019;60:631-48. [DOI: 10.1016/j.tetlet.2019.01.031] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 2.8] [Reference Citation Analysis]
10 Védrine JC. Metal Oxides in Heterogeneous Oxidation Catalysis: State of the Art and Challenges for a More Sustainable World. ChemSusChem 2019;12:577-88. [DOI: 10.1002/cssc.201802248] [Cited by in Crossref: 101] [Cited by in F6Publishing: 103] [Article Influence: 25.3] [Reference Citation Analysis]
11 Yamada M, Shio Y, Akiyama T, Honma T, Ohki Y, Takahashi N, Murai K, Arisawa M. Ligand-free Suzuki–Miyaura coupling reaction of an aryl chloride using a continuous irradiation type microwave and a palladium nanoparticle catalyst: effect of a co-existing solid. Green Chem 2019;21:4541-9. [DOI: 10.1039/c9gc01043b] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 1.8] [Reference Citation Analysis]
12 Yılmaz Baran N. Fabrication and characterization of a novel easy recoverable and reusable Oligoazomethine-Pd(II) catalyst for Suzuki cross-coupling reactions. Journal of Molecular Structure 2019;1176:266-74. [DOI: 10.1016/j.molstruc.2018.08.079] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 2.0] [Reference Citation Analysis]
13 Schroeter F, Soellner J, Strassner T. Cyclometalated Palladium NHC Complexes Bearing PEG Chains for Suzuki–Miyaura Cross-Coupling in Water. Organometallics 2018;37:4267-75. [DOI: 10.1021/acs.organomet.8b00607] [Cited by in Crossref: 16] [Cited by in F6Publishing: 17] [Article Influence: 3.2] [Reference Citation Analysis]
14 Luo K, Zhang L, Yang R, Jin Y, Lin J. Picolinamide modified β-cyclodextrin/Pd (II) complex: Asupramolecular catalyst for Suzuki-Miyaura coupling of aryl, benzyl and allyl halides with arylboronic acids in water. Carbohydrate Polymers 2018;200:200-10. [DOI: 10.1016/j.carbpol.2018.07.089] [Cited by in Crossref: 11] [Cited by in F6Publishing: 12] [Article Influence: 2.2] [Reference Citation Analysis]
15 Valange S, Védrine J. General and Prospective Views on Oxidation Reactions in Heterogeneous Catalysis. Catalysts 2018;8:483. [DOI: 10.3390/catal8100483] [Cited by in Crossref: 32] [Cited by in F6Publishing: 33] [Article Influence: 6.4] [Reference Citation Analysis]
16 Kang E, Shin H, Lim D. Interface-Controlled Pd Nanodot-Au Nanoparticle Colloids for Efficient Visible-Light-Induced Photocatalytic Suzuki-Miyaura Coupling Reaction. Catalysts 2018;8:463. [DOI: 10.3390/catal8100463] [Cited by in Crossref: 10] [Cited by in F6Publishing: 11] [Article Influence: 2.0] [Reference Citation Analysis]
17 Quapp W, Bofill JM, Ribas-ariño J. Toward a theory of mechanochemistry: Simple models from the very beginnings. Int J Quantum Chem 2018;118:e25775. [DOI: 10.1002/qua.25775] [Cited by in Crossref: 11] [Cited by in F6Publishing: 13] [Article Influence: 2.2] [Reference Citation Analysis]
18 Dilauro G, García SM, Tagarelli D, Vitale P, Perna FM, Capriati V. Ligand-Free Bioinspired Suzuki-Miyaura Coupling Reactions using Aryltrifluoroborates as Effective Partners in Deep Eutectic Solvents. ChemSusChem 2018;11:3495-501. [DOI: 10.1002/cssc.201801382] [Cited by in Crossref: 44] [Cited by in F6Publishing: 45] [Article Influence: 8.8] [Reference Citation Analysis]
19 Baran T. Pd(0) nanocatalyst stabilized on a novel agar/pectin composite and its catalytic activity in the synthesis of biphenyl compounds by Suzuki-Miyaura cross coupling reaction and reduction of o-nitroaniline. Carbohydrate Polymers 2018;195:45-52. [DOI: 10.1016/j.carbpol.2018.04.064] [Cited by in Crossref: 65] [Cited by in F6Publishing: 58] [Article Influence: 13.0] [Reference Citation Analysis]
20 Baran T. Ultrasound-accelerated synthesis of biphenyl compounds using novel Pd(0) nanoparticles immobilized on bio-composite. Ultrasonics Sonochemistry 2018;45:231-7. [DOI: 10.1016/j.ultsonch.2018.03.017] [Cited by in Crossref: 57] [Cited by in F6Publishing: 57] [Article Influence: 11.4] [Reference Citation Analysis]
21 Baran T, Yılmaz Baran N, Menteş A. Preparation, structural characterization, and catalytic performance of Pd(II) and Pt(II) complexes derived from cellulose Schiff base. Journal of Molecular Structure 2018;1160:154-60. [DOI: 10.1016/j.molstruc.2018.01.074] [Cited by in Crossref: 45] [Cited by in F6Publishing: 44] [Article Influence: 9.0] [Reference Citation Analysis]
22 You L, Cui L, Zhao B, Xiong G, Ding F, Ren B, Shi Z, Dragutan I, Dragutan V, Sun Y. Tailoring the structure, pH sensitivity and catalytic performance in Suzuki–Miyaura cross-couplings of Ln/Pd MOFs based on the 1,1′-di( p -carboxybenzyl)-2,2′-diimidazole linker. Dalton Trans 2018;47:8755-63. [DOI: 10.1039/c8dt01288a] [Cited by in Crossref: 16] [Cited by in F6Publishing: 16] [Article Influence: 3.2] [Reference Citation Analysis]
23 Baran T, Yılmaz Baran N, Menteş A. Sustainable chitosan/starch composite material for stabilization of palladium nanoparticles: Synthesis, characterization and investigation of catalytic behaviour of Pd@chitosan/starch nanocomposite in Suzuki–Miyaura reaction. Appl Organometal Chem 2018;32. [DOI: 10.1002/aoc.4075] [Cited by in Crossref: 52] [Cited by in F6Publishing: 53] [Article Influence: 8.7] [Reference Citation Analysis]