Библиография

1. 1. Zhang S., Ma H., Sun Y., Luo Y., Liu X., Zhang M., Gao J., Xu J. Catalytic selective hydrogenation and rearrangement of 5-hydroxymethylfurfural to 3-hydroxymethyl-cyclopentone over a bimetallic nickel-copper catalyst in water // Green Chem. 2019. V. 21. P. 1702-1709. https://doi.org/10.1039/C8GC04009E
2. 2. Zhang X., Du L., Xu Z. The effect of soft bake on adhesion property between SU-8 photoresist and Ni substrate by molecular dynamics simulation // J. Appl. Polym. Sci. 2013. V. 127. P. 4456-4462. https://doi.org/10.1002/app.38011
3. 3. Dutta S., Bhat N. S. Catalytic transformation of biomass-derived furfurals to cyclopentanones and their derivatives: A review // ACS Omega. 2021. V. 6. N 51. P. 35145-35172. https://doi.org/10.1021/acsomega.1c05861
4. 4. Gordillo Sierra A. R., Alper H. S. Progress in the metabolic engineering of bio-based lactams and their ω-amino acids precursors // Biotechnol. Adv. 2020. V. 43. ID 107587. https://doi.org/10.1016/j.biotechadv.2020.107587
5. 5. Renz M. Ketonization of carboxylic acids by decarboxylation: Mechanism and scope // Eur. J. Org. Chem. 2005. V. 6. P. 979-988. https://doi.org/10.1002/ejoc.200400546
6. 6. Pat. US 5856581 A (publ. 1999). Preparation of cyclic ketones.
7. 7. Date N. S., Kondawar S. E., Chikate R. C., Rode C. V. Single-pot reductive rearrangement of furfural to cyclopentanone over silica-supported Pd catalysts // ACS Omega. 2018. V. 3. P. 9860-9871. https://doi.org/10.1021/acsomega.8b00980
8. 8. Salnikova K. E., Larichev Y. V., Sulman E. M., Bykov A. V., Sidorov A. I., Demidenko G. N., Sulman M. G., Bronstein L. M., Matveeva V. G. Selective hydrogenation of biomass-derived furfural: Enhanced catalytic performance of Pd-Cu alloy nanoparticles in porous polymer // ChemPlusChem. 2020. V. 85. P. 1697-1703. https://doi.org/10.1002/cplu.202000383
9. 9. Duan Y., Cheng Y., Hu Z., Wang C., Sui D., Yang Y., Lu T. A comprehensive review on metal catalysts for the production of cyclopentanone derivatives from furfural and HMF // Molecules. 2023. V. 28. ID 5397. https://doi.org/10.3390/molecules28145397
10. 10. Бороноев М. П., Шакиров И. И., Ролдугина Е. А., Кардашева Ю. С., Кардашев С. В. Гидрирование фурфурола в присутствии Ru и Pd катализаторов, иммобилизованных на гибридных материалах на основе мезопористых фенолформальдегидных полимеров и оксида кремния // ЖПХ. 2023. T. 96. № 11. C. 857-865. https://doi.org/10.31857/S0044461823110038
11. 11. Boronoev M. P., Shakirov I. I., Roldugina E. A., Kardasheva Yu. S., Kardashev S. V. Furfural hydrogenation in the presence of Ru and Pd catalysts immobilized on hybrid materials based on mesoporous phenol-formaldehyde polymers and silica //Russ. J. Appl. Chem. 2023. V. 96. N 10. P. 944-952. https://doi.org/10.1134/S1070427223110036
12. 12. Morales M. V., Conesa J. M., Campos-Castellanos E., Guerrero-Ruiz A. Rodríguez-Ramos I. Critical factors affecting the selective transformation of 5-hydroxymethylfurfural to 3-hydroxymethylcyclopentanone over Ni catalysts // ChemSusChem. 2024. V. 17. N 23. ID e202400559. https://doi.org/10.1002/cssc.202400559
13. 13. Dragoi B., Dumitriu E., Guimon C., Auroux A. Acidic and adsorptive properties of SBA-15 modified by aluminum incorporation // Micropor. Mesopor. Mater. 2009. V. 121. P. 7-17. https://doi.org/10.1016/j.micromeso.2008.12.023
14. 14. Zhang F., Liang C., Wu X., Li H. A nanospherical ordered mesoporous Lewis acid polymer for the direct glycosylation of unprotected and unactivated sugars in water // Angew. Chem.Int. Ed. 2014. V. 53. N 32. P. 8498-502. https://doi.org/10.1002/anie.201404353
15. 15. Kumaran G. M., Garg S., Soni K., Kumar M., Gupta J. K., Sharma L. D., Rao K. S. R., Dhar G. M. Synthesis and characterization of acidic properties of Al-SBA-15 materials with varying Si/Al ratios // Micropor. Mesopor. Mater. 2008. V. 114. P. 103-109. https://doi.org/10.1016/j.micromeso.2007.12.021
16. 16. Meng Y., Gu D., Zhang F., Shi Y., Yang H., Li Z., Yu C., Tu B., Zhao D. Ordered mesoporous polymers and homologous carbon frameworks: Amphiphilic surfactant templating and direct transformation // Angew. Chem.Int. Ed. 2005. V. 44. N. 43. P. 7053- 7059. https://doi.org/10.1002/anie.200501561
17. 17. Ролдугина Е. А., Бороноев М. П., Шакиров И. И., Кардашева Ю. С., Кардашев С. В. Гидрирование фурфурола, 5-гидроксиметилфурфурола и левулиновой кислоты в присутствии Pd катализатора, нанесенного на мезопористый цирконосиликат // ЖПХ. 2024. T. 97. № 1. C. 63-69. https://doi.org/10.31857/S0044461824010080
18. 18. Li X., Tong Z., Zhu S., Deng Q., Chen S., Wang J., Zeng Z., Zhang Y., Zou J., Deng S. Water-mediated hydrogen spillover accelerates hydrogenative ringrearrangement of furfurals to cyclic compounds // J. Catal. 2022. V. 405. P. 363-372. https://doi.org/10.1016/j.jcat.2021.12.010
19. 19. Ohyama J., Kanao R., Ohira Y., Satsuma A. The effect of heterogeneous acid-base catalysis on conversion of 5-hydroxymethylfurfural into a cyclopentanone derivative // Green Сhem. 2016. V. 18. N 3. P. 676- 680. https://doi.org/10.1039/C5GC01723H
20. 20. Ohyama J., Ohira Y., Satsuma A. Hydrogenative ringrearrangement of biomass derived 5-(hydroxymethyl)-furfural to 3-(hydroxymethyl)cyclopentanol using combination catalyst systems of Pt/SiO2 and lanthanoid oxides // Catal. Sci. Technol. 2017. V. 7. P. 2947-2953. https://doi.org/10.1039/C7CY00712D