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Chemsuschem, 1864-5631

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1 - 38 out of 38Page size: 50
  1. 2020
  2. Sun, Z., Cheng, J., Wang, D., Yuan, T-Q., Song, G., & Barta, K. (2020). Downstream Processing Strategies for Lignin-First Biorefinery. Chemsuschem, 13(19), 5199-5212. https://doi.org/10.1002/cssc.202001085
  3. Lahive, C. W., Kamer, P. C. J., Lancefield, C. S., & Deuss, P. J. (2020). An Introduction to Model Compounds of Lignin Linking Motifs; Synthesis and Selection Considerations for Reactivity Studies. Chemsuschem, 13(17), 4238-4265. https://doi.org/10.1002/cssc.202000989
  4. De Santi, A., Galkin, M. V., Lahive, C. W., Deuss, P. J., & Barta, K. (2020). Lignin-First Fractionation of Softwood Lignocellulose Using a Mild Dimethyl Carbonate and Ethylene Glycol Organosolv Process. Chemsuschem, 13(17), 4468-4477. https://doi.org/10.1002/cssc.201903526
  5. 2019
  6. Abdilla-Santes, R. M., Guo, W., Bruijnincx, P. C. A., Yue, J., Deuss, P. J., & Heeres, H. J. (2019). High-Yield 5-Hydroxymethylfurfural Synthesis from Crude Sugar Beet Juice in a Biphasic Microreactor. Chemsuschem, 12(18), 4304-4312. https://doi.org/10.1002/cssc.201901115
  7. Afanasenko, A., Hannah, R., Yan, T., Elangovan, S., & Barta, K. (2019). Ruthenium and Iron-Catalysed Decarboxylative N-alkylation of Cyclic α-Amino Acids with Alcohols: Sustainable Routes to Pyrrolidine and Piperidine Derivatives. Chemsuschem, 12(16), 3801-3807. https://doi.org/10.1002/cssc.201901499
  8. Alassmy, Y. A., & Pescarmona, P. P. (2019). The Role of Water Revisited and Enhanced: A Sustainable Catalytic System for the Conversion of CO2 into Cyclic Carbonates under Mild Conditions. Chemsuschem, 12(16), 3856-3863. https://doi.org/10.1002/cssc.201901124
  9. Kamphuis, A. J., Milocco, F., Koiter, L., Pescarmona, P., & Otten, E. (2019). Highly selective single-component formazanate ferrate(II) catalysts for the conversion of CO2 into cyclic carbonates. Chemsuschem, 12(15), 3635-3641. https://doi.org/10.1002/cssc.201900740
  10. Barbieri, A., Kasper, J. B., Mecozzi, F., Lanzalunga, O., & Browne, W. R. (2019). Origins of Catalyst Inhibition in the Manganese-Catalysed Oxidation of Lignin Model Compounds with H2O2. Chemsuschem, 12(13), 3126-3133. https://doi.org/10.1002/cssc.201900689
  11. Assil-Companioni, L., Schmidt, S., Heidinger, P., Schwab, H., & Kourist, R. (2019). Hydrogen-Driven Cofactor Regeneration for Stereoselective Whole-Cell C=C Bond Reduction in Cupriavidus necator. Chemsuschem, 12(11), 2361-2365. https://doi.org/10.1002/cssc.201900327
  12. Maniar, D., Jiang, Y., Woortman, A. J. J., van Dijken, J., & Loos, K. (2019). Furan-Based Copolyesters from Renewable Resources: Enzymatic Synthesis and Properties. Chemsuschem, 12(5), 990-999. https://doi.org/10.1002/cssc.201802867
  13. Aumala, V., Mollerup, F., Jurak, E., Blume, F., Karppi, J., Koistinen, A. E., Schuiten, E., Voss, M., Bornscheuer, U., Deska, J., & Master, E. R. (2019). Biocatalytic Production of Amino Carbohydrates through Oxidoreductase and Transaminase Cascades. Chemsuschem, 12(4), 848-857. https://doi.org/10.1002/cssc.201802580
  14. 2018
  15. Pinxterhuis, E. B., Gualtierotti, J-B., Wezenberg, S. J., de Vries, J. G., & Feringa, B. L. (2018). Highly Efficient and Robust Enantioselective Liquid-Liquid Extraction of 1,2-Amino Alcohols utilizing VAPOL- and VANOL-based Phosphoric Acid Hosts. Chemsuschem, 11(1), 178-184. https://doi.org/10.1002/cssc.201701896
  16. 2017
  17. Taherimehr, M., Van de Voorde, B., Wee, L. H., Martens, J. A., De Vos, D. E., & Pescarmona, P. (2017). Strategies for enhancing the catalytic performance of Metal-Organic Frameworks in the fixation of CO2 into cyclic carbonates. Chemsuschem, 10(6), 1283-1291. https://doi.org/10.1002/cssc.201601768
  18. 2016
  19. Galkin, M. V., Smit, A. T., Subbotina, E., Artemenko, K. A., Bergquist, J., Huijgen, W. J. J., & Samec, J. S. M. (2016). Hydrogen-free catalytic fractionation of woody biomass. Chemsuschem, 9(23), 3280-3287. https://doi.org/10.1002/cssc.201600648
  20. Deuss, P. J., Lahive, C. W., Lancefield, C. S., Westwood, N. J., Kamer, P. C. J., Barta, K., & de Vries, J. G. (2016). Metal Triflates for the Production of Aromatics from Lignin. Chemsuschem, 9(20), 2974-2981. https://doi.org/10.1002/cssc.201600831
  21. Yan, T., & Barta, K. (2016). Sustainable Pathways to Pyrroles through Iron-Catalyzed N-Heterocyclization from Unsaturated Diols and Primary Amines. Chemsuschem, 9(17), 2321-2325. https://doi.org/10.1002/cssc.201600607
  22. van Putten, R-J., van der Waal, J. C., Harmse, M., van de Bovenkamp, H. H., de Jong, E., & Heeres, H. J. (2016). A Comparative Study on the Reactivity of Various Ketohexoses to Furanics in Methanol. Chemsuschem, 9(14), 1827-1834. https://doi.org/10.1002/cssc.201600252
  23. Galkin, M. V., & Samec, J. S. M. (2016). Lignin Valorization through Catalytic Lignocellulose Fractionation: A Fundamental Platform for the Future Biorefinery. Chemsuschem, 9(13), 1544-1558. https://doi.org/10.1002/cssc.201600237
  24. Löfstedt, J., Dahlstrand, C., Orebom, A., Meuzelaar, G., Sawadjoon, S., Galkin, M. V., Agback, P., Wimby, M., Corresa, E., Mathieu, Y., Sauvanaud, L., Eriksson, S., Corma, A., & Samec, J. S. M. (2016). Green Diesel from Kraft Lignin in Three Steps. Chemsuschem, 9(12), 1392-1396. https://doi.org/10.1002/cssc.201600172
  25. Wang, Y., Agarwal, S., Kloekhorst, A., & Heeres, H. J. (2016). Catalytic Hydrotreatment of Humins in Mixtures of Formic Acid/2-Propanol with Supported Ruthenium Catalysts. Chemsuschem, 9(9), 951-961. https://doi.org/10.1002/cssc.201501371
  26. 2015
  27. Galkin, M. V., Dahlstrand, C., & Samec, J. S. M. (2015). Mild and Robust Redox-Neutral Pd/C-Catalyzed Lignol β-O-4' Bond Cleavage Through a Low-Energy-Barrier Pathway. Chemsuschem, 8(13). https://doi.org/10.1002/cssc.201500750
  28. Galkin, M. V., Dahlstrand, C., & Samec, J. S. M. (2015). Mild and Robust Redox-Neutral Pd/C-Catalyzed Lignol β-O-4′ Bond Cleavage Through a Low-Energy-Barrier Pathway. Chemsuschem, 8(13), 2187-2192. https://doi.org/10.1002/cssc.201500117
  29. Bottari, G., Kumalaputri, A. J., Krawczyk, K. K., Feringa, B. L., Heeres, H. J., & Barta, K. (2015). Copper-Zinc Alloy Nanopowder: A Robust Precious-Metal-Free Catalyst for the Conversion of 5-Hydroxymethylfurfural. Chemsuschem, 8(8), 1323-1327. https://doi.org/10.1002/cssc.201403453
  30. Taherimehr, M., Sertã, J. P. C. C., Kleij, A. W., Whiteoak, C. J., & Pescarmona, P. P. (2015). New iron pyridylamino-bis(phenolate) catalyst for converting CO2 into cyclic carbonates and cross-linked polycarbonates. Chemsuschem, 8(6), 1034-1042. https://doi.org/10.1002/cssc.201403323
  31. 2014
  32. Kumalaputri, A. J., Bottari, G., Erne, P. M., Heeres, H. J., & Barta, K. (2014). Tunable and selective conversion of 5-HMF to 2,5-furandimethanol and 2,5-dimethylfuran over copper-doped porous metal oxides. Chemsuschem, 7(8), 2266-2275. https://doi.org/10.1002/cssc.201402095
  33. Pazhavelikkakath Purushothaman, R. K., van Haveren, J., Melian Cabrera, I., van Eck, E. R. H., & Heeres, H. J. (2014). Base-Free, One-Pot Chemocatalytic Conversion of Glycerol to Methyl Lactate using Supported Gold Catalysts. Chemsuschem, 7(4), 1140-1147. https://doi.org/10.1002/cssc.201301105
  34. Galkin, M. V., & Samec, J. S. M. (2014). Selective route to 2-propenyl aryls directly from wood by a tandem organosolv and palladium-catalysed transfer hydrogenolysis. Chemsuschem, 7(8), 2154-2158. https://doi.org/10.1002/cssc.201402017
  35. 2013
  36. van Putten, R-J., Soetedjo, J. N. M., Pidko, E. A., van der Waal, J. C., Hensen, E. J. M., de Jong, E., & Heeres, H. J. (2013). Dehydration of Different Ketoses and Aldoses to 5-Hydroxymethylfurfural. Chemsuschem, 6(9), 1681-1687. https://doi.org/10.1002/cssc.201300345
  37. Gottumukkala, A. L., Suljagic, J., Matcha, K., de Vries, J. G., & Minnaard, A. J. (2013). Efficient Formation of Benzylic Quaternary Centers via Palladium Catalysis. Chemsuschem, 6(9), 1636-1639. https://doi.org/10.1002/cssc.201300276
  38. van Zandvoort, I., Wang, Y., Rasrendra, C. B., van Eck, E. R. H., Bruijnincx, P. C. A., Heeres, H. J., & Weckhuysen, B. M. (2013). Formation, Molecular Structure, and Morphology of Humins in Biomass Conversion: Influence of Feedstock and Processing Conditions. Chemsuschem, 6(9), 1745-1758. https://doi.org/10.1002/cssc.201300332
  39. Dong, J. J., Unjaroen, D., Mecozzi, F., Harvey, E. C., Saisaha, P., Pijper, D., de Boer, J. W., Alsters, P., Feringa, B. L., & Browne, W. R. (2013). Manganese-Catalyzed Selective Oxidation of Aliphatic C-H groups and Secondary Alcohols to Ketones with Hydrogen Peroxide. Chemsuschem, 6(9), 1774-1778. https://doi.org/10.1002/cssc.201300378
  40. Nicklaus, C. M., Minnaard, A. J., Feringa, B. L., & de Vries, J. G. (2013). Synthesis of Renewable Fine-Chemical Building Blocks by Reductive Coupling between Furfural Derivatives and Terpenes. Chemsuschem, 6(9), 1631-1635. https://doi.org/10.1002/cssc.201300179
  41. 2012
  42. Perdriau, S., Harder, S., Heeres, H. J., & de Vries, J. G. (2012). Selective Conversion of Polyenes to Monoenes by RuCl3-Catalyzed Transfer Hydrogenation: The Case of Cashew Nutshell Liquid. Chemsuschem, 5(12), 2427-2434. https://doi.org/10.1002/cssc.201200503
  43. 2011
  44. Aprile, C., Giacalone, F., Agrigento, P., Liotta, L. F., Martens, J. A., Pescarmona, P. P., & Gruttadauria, M. (2011). Multilayered Supported Ionic Liquids as Catalysts for Chemical Fixation of Carbon Dioxide: A High-Throughput Study in Supercritical Conditions. Chemsuschem, 4(12), 1830-1837. https://doi.org/10.1002/cssc.201100446
  45. Jammaer, J., Aprile, C., Verbruggen, S. W., Lenaerts, S., Pescarmona, P. P., & Martens, J. A. (2011). A Non-Aqueous Synthesis of TiO2/SiO2 Composites in Supercritical CO2 for the Photodegradation of Pollutants. Chemsuschem, 4(10), 1457-1463. https://doi.org/10.1002/cssc.201100059
  46. Philippaerts, A., Goossens, S., Vermandel, W., Tromp, M., Turner, S., Geboers, J., Van Tendeloo, G., Jacobs, P. A., & Sels, B. F. (2011). Design of Ru-Zeolites for Hydrogen-Free Production of Conjugated Linoleic Acids. Chemsuschem, 4(6), 757-767. https://doi.org/10.1002/cssc.201100015
  47. Rasrendra, C. B., Fachri, B. A., Makertihartha, I. G. B. N., Adisasmito, S., & Heeres, H. J. (2011). Catalytic Conversion of Dihydroxyacetone to Lactic Acid Using Metal Salts in Water. Chemsuschem, 4(6), 768-777. https://doi.org/10.1002/cssc.201000457
  48. 2008
  49. Li, C., Yum, J-H., Moon, S-J., Herrmann, A., Eickemeyer, F., Pschirer, N. G., Erk, P., Schoeneboom, J., Muellen, K., Graetzel, M., Nazeeruddin, M. K., Müllen, K., & Grätzel, M. (2008). An Improved Perylene Sensitizer for Solar Cell Applications. Chemsuschem, 1(7), 615-618. https://doi.org/10.1002/cssc.200800068

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