Publications - Dr. Eszter Baráth
49. | Li, Katja; Kelly, H. Ray; Franco, Ana; Batista, Victor S.; Baráth, Eszter ACS Catalysis, , 2883-2896. Dehydrogenation and Transfer Hydrogenation of Alkenones to Phenols and Ketones on Carbon-Supported Noble Metals. |
48. | Yue, Xiaoyang; Cheng, Lei; Baráth, Eszter; Jagadeesh, Rajenahally V.; Xiang, Quanjun Electron, , n/a, e16. Deciphering orbital hybridization in heterogeneous catalysis. |
47. | Chakrabortty, Soumyadeep; Konieczny, Katharina; de Zwart, Felix J.; Bobylev, Eduard. O.; Baráth, Eszter; Tin, Sergey; Müller, Bernd H.; Reek, Joost N. H.; de Bruin, Bas; de Vries, Johannes G. Angewandte Chemie, , n/a, e202301329. Cobalt-katalysierte enantioselektive Hydrierung von dreifach substituierten carbocyclischen Olefinen: Zugang zu chiralen cyclischen Amiden. |
46. | Chakrabortty, Soumyadeep; Zheng, Shasha; Kallmeier, Fabian; Baráth, Eszter; Tin, Sergey; de Vries, Johannes G. ChemSusChem, , 16, e202202353. Ru-Catalyzed Direct Asymmetric Reductive Amination of Bio-Based Levulinic Acid and Ester for the Synthesis of Chiral Pyrrolidinone. |
45. | Gupta, Priyanka; Drexler, Hans-Joachim; Wingad, Richard; Wass, Duncan; Baráth, Eszter; Beweries, Torsten; Hering-Junghans, Christian Inorganic Chemistry Frontiers, , 10, 2285-2293. P,N-type phosphaalkene-based Ir(i) complexes: synthesis, coordination chemistry, and catalytic applications. |
44. | Mazloomi, Zahra; Kallmeier, Fabian; Kirchhecker, Sarah; Stadler, Bernhard M.; Pandey, Swechchha; Schünemann, Claas; Spannenberg, Anke; Hering-Junghans, Christian; Tin, Sergey; de Vries, Johannes G.; Baráth, Eszter Chemical Communications, , 59, 8444-8447. Unusual selectivity in the ring-opening of γ-valerolactone oxide by amines. |
43. | Liu, Qiang; Pfriem, Niklas; Cheng, Guanhua; Baráth, Eszter; Liu, Yue; Lercher, Johannes A. Angewandte Chemie International Edition, , 62, e202208693. Maximum Impact of Ionic Strength on Acid-Catalyzed Reaction Rates Induced by a Zeolite Microporous Environment. |
42. | Zheng, Shasha; Wei, Zhihong; Wozniak, Bartosz; Kallmeier, Fabian; Baráth, Eszter; Jiao, Haijun; Tin, Sergey; de Vries, Johannes G. Nature Sustainability, , Synthesis of valuable benzenoid aromatics from bioderived feedstock. |
41. | Milaković, Lara; Liu, Yue; Baráth, Eszter; Lercher, Johannes A. Catalysis Science & Technology, , 12, 6084-6091. Dehydration of fatty alcohols on zirconia supported tungstate catalysts. |
40. | Senthamarai, Thirusangumurugan; Poovan, Fairoosa; Alenad, Asma M.; Rockstroh, Nils; Rabeah, Jabor; Bartling, Stephan; Baráth, Eszter; Natte, Kishore; Jagadeesh, Rajenahally V. Advanced Sustainable Systems, , n/a, 2200263. Cu-Oxide Nanoparticles Catalyzed Synthesis of Nitriles and Amides from Alcohols and Ammonia in Presence of Air. |
39. | Flynn, Matthew T.; Liu, Xin; Dell'Acqua, Andrea; Rabeah, Jabor; Brueckner, Angelika; Baráth, Eszter; Tin, Sergey; de Vries, Johannes G. ChemSusChem, , n/a, e202201264. Glycolaldehyde as a Bio-Based C1 Building Block for Selective N-Formylation of Secondary Amines. |
38. | Zheng, Shasha; Chakrabortty, Soumyadeep; Baráth, Eszter; Tin, Sergey; de Vries, Johannes G. ACS Sustainable Chemistry & Engineering, , 10, 15642-15647. Synthesis of N-Substituted 3-Hydroxypyridinium Salts from Bioderived 5-Hydroxymethylfurfural in Water. |
37. | Dell’Acqua, Andrea; Schünemann, Claas; Baráth, Eszter; Tin, Sergey; de Vries, Johannes G. Chemical Communications, , 58, 13091-13094. New bifunctional monomers from methyl vinyl glycolate. |
36. | Liu, Xin; Zuo, Yujing; Kallmeier, Fabian; Mejía, Esteban; Tin, Sergey; de Vries, Johannes G.; Baráth, Eszter Chemical Communications, , 58, 5415-5418. Hydrogenative depolymerization of silicon-modified polyureas. |
35. | Rate enhancement of phenol hydrogenation on Pt by hydronium ions in the aqueous phase Yang, G.; Maliekkal, V.; Chen, X.; Eckstein, S.; Shi, H.; Camaioni, D. M.; Baráth, E.; Haller, G. L.; Liu, Y.; Neurock, M.; Lercher, J. A., J. Catal. 2021, 404, 579-593. |
34. | Influence of intracrystalline ionic strength in MFI zeolites on aqueous phase dehydration of methylcyclohexanols Milakovic, L.; Hintermeier, P. H.; Liu, Y.; Baráth, E.; Lercher, J. A., Angew. Chem. Int. Ed. 2021, 60, 24806-24810. |
33. | Role of the ionic environment to enhance activity of reacting molecules in zeolite pores Pfriem, N.; Hintermeier, P. H.; Eckstein, S.; Kim, S.; Liu, Q.; Shi, H.; Milakovic, L.; Liu, Y.; Haller, G. L.; Baráth, E.; Liu, Y.; Lercher, J. A., Science 2021, 372, 952-957. |
32. | Selective heterogeneous transfer hydrogenation from tertiary amines to alkynes Roeder, G. J.; Kelly, R. H.; Yang, G.; Bauer, T. J.; Haller, G. L.; Batista, V. S.; Baráth, E. ,ACS Catal. 2021, 11, 5405-5415. |
31. | Alkylation of lignin-derived aromatic oxygenates with cyclic alcohols on acidic zeolites Liu, Y.; Cheng, G.; Baráth, E.; Shi, H.; Lercher, J. A. Appl. Catal. B: Environ. 2021, 281, 119424. |
30. | Towards understanding and predicting the hydronium ion catalyzed dehydration of cyclic- primary, secondary and tertiary alcohols Milakovic, L.; Hintermeier, P. H.; Liu, Q.; Shi, H.; Liu, Y.; Baráth, E.; Lercher, J. A., J. Catal. 2020, 390, 237-243. |
29. | Selective conversion of C=O bond via (asymmetric) transfer hydrogenation on heterogeneous catalysts (Review) Baráth, E., Synthesis, 2020, 52, 504-520. (in the special issue “Future Stars in Organic Chemistry” of the JSP fellows of the 54th Bürgenstock Conference). |
28. | A celebration of science amidst nature: The 54th Bürgenstock Conference (Conference review) Baráth, E.; Mejía, E., Angew. Chem. Int. Ed. 2019, 58, 2-10. |
27. | Rate enhancement by Cu in NixCu1-x/ZrO2 bimetallic catalysts for hydrodeoxygenation of stearic acid Denk, C.; Foraita, S.; Kovarik, L.; Stoerzinger, K.; Liu, Y.; Baráth, E.; Lercher, J. A., Catal. Sci. Technol. 2019, 9, 2620-2629. |
26. | Catalytic decomposition of the oleaginous yeast Cutaneotrichosporon Oleaginosus and subsequent biocatalytic conversion of liberated free fatty acids Braun, M. K.; Lorenzen, J.; Masri, M.; Liu, Y.; Baráth, E.; Brück, T.; Lercher, J. A., ACS Sustainable Chem. Eng. 2019, 7, 6531-6540. |
25. | Influence of hydronium ions in zeolites on sorption Eckstein, S.; Hintermeier, P. H.; Zhao, R.; Baráth, E.; Shi, H.; Liu, Y.; Lercher, J. A., Angew. Chem. Int. Ed. 2019, 58, 1-7. |
24. | Hydrogen transfer reactions of carbonyls, alkynes, and alkenes with noble metals in the presence of alcohols/ethers and amines as hydrogen donors (Review) Baráth, E., Catalysts 2018, 8, 671-696. |
23. | Solvent determined mechanistic pathways in zeolite H-BEA catalyzed phenol alkylation Liu, Y.; Baráth, E.; Shi, H.; Hu, J.; Camaioni, D. M.; Lercher, J. A., Nature Catal. 2018, 1, 141–147. (http://rdcu.be/FQ1Q) |
22. | H-Transfer reactions of internal alkenes with tertiary amines as H-donors on carbon supported noble metals Yang, G.; Bauer, T. J.; Haller, G. L.; Baráth, E. Org. Biomol. Chem. 2018, 16, 1172-1177. |
21. | Hydronium-ion-catalyzed elimination pathways of substituted cyclohexanols in zeolite H-ZSM5 Hintermeier, P. H.; Eckstein, S.; Mei, D.; Olarte, M. V.; Camaioni, D. M.; Baráth, E.; Lercher, J. A., ACS Catal. 2017, 7, 7822-7829. |
20. | Deoxygenation of palmitic acid on unsupported transition metal phosphides Peroni, M.; Lee, I.; Huang, X.; Baráth, E.; Gutiérrez, O.; Lercher, J. A., ACS Catal. 2017, 7, 6331-6341. |
19. | Elementary steps and reaction pathways in the aqueous phase alkylation of phenol with ethanol Eckstein, S.; Hintermeier, P. H.; Olarte, M. V.; Liu, Y.; Baráth, E.; Lercher, J. A., J. Catal. 2017, 352, 329-336. |
18. | Enhancing the catalytic activity of hydronium ions through constrained environments Liu, Y.; Vjunov, A.; Shi, H.; Eckstein, S.; Camaioni, D. M.; Mei, D.; Baráth, E.; Lercher, J. A., Nature Commun. 2017, 8, 14113. |
17. | Acid-base controlled carbon-carbon bond scission pathways in the deoxygenation of fatty acids on transition metal sulfides Wagenhofer, M. F.; Baráth, E.; Gutiérrez, O. Y.; Lercher, J. A., ACS Catal. 2017, 7, 1068-1076. |
16. | Controlling hydrodeoxygenation of stearic acid to n-heptadecane and n-octadecane by adjusting the chemical properties of Ni/SiO2-ZrO2 catalyst Foraita, S.; Liu, Y.; Haller, G. L.; Baráth, E.; Zhao, C.; Lercher, J. A., ChemCatChem 2017, 9, 195-203. |
15. | Dehydration of 1-octadecanol over H-BEA: A combined experimental and computational study Song, W.; Liu, Y.; Baráth, E.; Wang, L.; Zhao, C.; Mei, D.; Lercher, J. A., ACS Catal. 2016, 6, 878-889. |
14. | Bulk and γ-Al2O3-supported Ni2P and MoP for hydrodeoxygenation of palmitic acid Peroni, M.; Mancino, G.; Baráth, E.; Gutiérrez, O. Y.; Lercher, J. A., Appl. Catal. B: Environ. 2016, 180, 301-311. |
13. | Reductive deconstruction of organosolv lignin catalyzed by zeolite supported nickel nanoparticles Kasakov, S.; Shi, H.; Camaioni, D.; Zhao, C.; Baráth, E.; Jentys, A.; Lercher, J. A., Green Chem. 2015, 17, 5079-5090. |
12. | Rh-catalyzed hydroformylation of 1,3-butadiene to adipic aldehyde: Revealing selectivity and rate determining steps Schmidt, S.; Baráth, E.; Larcher, C.; Rosendahl, T.; Hofmann, P., Organometallics 2015, 34, 841-847. |
11. | Synergistic effects of Ni and acid sites for hydrogenation and C−O bond cleavage of substituted phenols Song, W.; Liu, Y.; Baráth, E.; Zhao, C.; Lercher, J. A., Green Chem. 2015, 17, 1204-1218 |
10. | Glucose and cellulose derived Ni/C-SO3H catalysts for liquid phase phenol hydrodeoxygenation Kasakov, S.; Zhao, C.; Baráth, E.; Chase, Z. A.; Fulton, J. L.; Camaioni, D. M.; Vjunov, A.; Shi, H.; Lercher, J. A., Chem. Eur. J. 2015, 21, 1567-1577. |
9. | Impact of the oxygen defects and the hydrogen concentration on the surface of tetragonal and monoclinic ZrO2 on the reduction rates of stearic acid on Ni/ZrO2 Foraita, S.; Fulton, J. L.; Chase, Z. A.; Vjunov, A.; Xu, P.; Baráth, E.; Camaioni, D. M.; Zhao, C.; Lercher, J. A., Chem. Eur. J. 2015, 21, 2423-2434. |
8. | Synthesis and characterization of crotyl intermediates in Rh-catalyzed hydroformylation of 1,3-butadiene Schmidt, S.; Baráth, E.; Prommnitz, T.; Rosendahl, T.; Rominger, F.; Hofmann, P., Organometallics, 2014, 33, 6018-6022. |
7. | Rhenium complexes bearing phosphole-pyridine chelates: simple molecules with large chiroptical properties Takács, E.; Escande, A.; Vanthuyne, N.; Roussel, C.; Lescop, C.; Guinard, E.; Latouche, C.; Boucekkine, A.; Crassous, J.; Réau, R.; Hissler, M., Chem. Commun. 2012, 48, 6705-6707. |
6. | Synthesis of new steroidal derivatives by the reaction of steroid ― amino acid conjugates with N,N’-dicyclohexyl-carbodiimide – Unusual formation of steroidal imide derivatives Takács, E.; Háda, V.; Mahó, S.; Berente, Z.; Kollár, L.; Skoda-Földes, R., Tetrahedron 2009, 65, 4659-4663. |
5. | Investigation of the effect of the ligand/palladium ratio on the catalytic activity of reusable palladium / phosphine / ionic liquid systems in aminocarbonylation of 17-iodo-androst-16-ene with amino acid ester nucleophiles Takács, E.; Skoda-Földes, R., Lett. Org. Chem. 2009, 6, 448-452. |
4. | Facile synthesis of primary amides and ketoamides via a palladium-catalysed carbonylation – deprotection reaction sequence Takács, E.; Varga, Cs.; Skoda-Földes, R.; Kollár, L., Tetrahedron Lett. 2007, 48, 2453-2456. |
3. | Prolinates as secondary amines in aminocarbonylation: synthesis of N-acylated prolinates Takács, E.; Skoda-Földes, R.; Ács, P.; Müller, E.; Kokotos, G.; Kollár, L., Lett. Org. Chem. 2006, 3, 62-67. |
2. | Homogeneous catalytic aminocarbonylation of iodoalkenes and iodobenzene with amino acid esters under conventional conditions and in ionic liquids Müller, E.; Péczely, G.; Skoda-Földes, R.; Takács, E.; Kokotos, G.; Bellis, E.; Kollár, L., Tetrahedron 2005, 61, 797-802. |
1. | Palladium-catalysed aminocarbonylation of steroidal 17-iodo-androst-16-ene derivatives in N,N’-dialkyl-imidazolium-type ionic liquids Skoda-Földes, R.; Takács, E.; Horváth, J.; Tuba, Z.; Kollár, L., Green Chem. 2003, 5, 643-645. |