Biomass Valorization. Группа авторов

production of lactic acid from cellulose using lanthanide triflate catalysts. Green Chemistry 15: 2091–2095.

      105 105. Verma, D., Insyani, R., Suh, Y.‐W. et al. (2017). Direct conversion of cellulose to high‐yield methyl lactate over Ga‐doped Zn/H‐nanozeolite Y catalysts in supercritical methanol. Green Chemistry 19: 1969–1982.

      106 106. Yang, L., Yang, X., Tian, E., and Lin, H. (2016). Direct conversion of cellulose into ethyl lactate in supercritical ethanol–water solutions. ChemSusChem 9 (1): 36–41.

      107 107. Zan, Y., Sun, Y., Kong, L. et al. (2018). Formic acid‐induced controlled‐release hydrolysis of microalgae (Scenedesmus) to lactic acid over Sn‐beta catalyst. ChemSusChem 11 (15): 2492–2496.

      108 108. De Clercq, R., Dusselier, M., and Sels, B.F. (2017). Heterogeneous catalysis for bio‐based polyester monomers from cellulosic biomass: advances, challenges and prospects. Green Chemistry 19: 5012–5040.

      109 109. Anderson, E.M., Stone, M.L., Katahira, R. et al. (2019). Differences in S/G ratio in natural poplar variants do not predict catalytic depolymerization monomer yields. Nature Communications https://doi.org/10.1038/s41467-019-09986-1.

      110 110. Calvo‐Flores, F.G. and Dobado, J.A. (2010). Lignin as renewable raw material. ChemSusChem 3: 1227–1235.

      111 111. Bozell, J.J. (2014). Approaches to the selective catalytic conversion of lignin: a grand challenge for biorefinery development. In: Selective Catalysis for Renewable Feedstocks and Chemicals (ed. K.M. Nicholas), 229–255. Cham: Springer.

      112 112. Anderson, E.M., Stone, M.L., Katahira, R. et al. (2017). Flowthrough reductive catalytic fractionation of biomass. Joule 1 (3): 613–622.

      113 113. Deuss, P.J., Lahive, C.W., Lancefield, C.S. et al. (2016). Metal triflates for the production of aromatics from lignin. ChemSusChem 9 (20): 2974–2981.

      114 114. Miles‐Barrett, D.M., Neal, A.R., Hand, C. et al. (2016). The synthesis and analysis of lignin‐bound Hibbert ketone structures in technical lignins. Organic & Biomolecular Chemistry 14: 10023–10030.

      115 115. Williams, D.B.G., Shaw, M.L., Green, M.J., and Holzapfel, C.W. (2008). Aluminum triflate as a highly active and efficient nonprotic cocatalyst in the palladium‐catalyzed methoxycarbonylation reaction. Angewandte Chemie International Edition 47 (3): 560–563.

      116 116. Williams, D.B.G. and Lawton, M. (2005). Aluminium triflate: a remarkable Lewis acid catalyst for the ring opening of epoxides by alcohols. Organic & Biomolecular Chemistry 3: 3269–3272.

      117 117. Deuss, P.J., Lancefield, C.S., Narani, A. et al. (2017). Phenolic acetals from lignins of varying compositions via iron(III) triflate catalysed depolymerisation. Green Chemistry 19: 2774–2782.

      118 118. Binder, J.B., Gray, M.J., White, J.F. et al. (2009). Reactions of lignin model compounds in ionic liquids. Biomass and Bioenergy 33 (9): 1122–1130.

      119 119. Cox, B.J., Jia, S., Zhang, Z.C., and Ekerdt, J.G. (2011). Catalytic degradation of lignin model compounds in acidic imidazolium based ionic liquids: Hammett acidity and anion effects. Polymer Degradation and Stability 96 (4): 426–431.

      120 120. Jia, S., Cox, B.J., Guo, X. et al. (2010). Cleaving the β‐O‐4 bonds of lignin model compounds in an acidic ionic liquid, 1‐H‐3‐methylimidazolium chloride: an optional strategy for the degradation of lignin. ChemSusChem 3 (9): 1078–1084.

      121 121. Jia, S., Cox, B.J., Guo, X. et al. (2011). Hydrolytic cleavage of β‐O‐4 ether bonds of lignin model compounds in an ionic liquid with metal chlorides. Industrial and Engineering Chemistry Research 50 (2): 849–855.

      122 122. Scott, M., Deuss, P.J., de Vries, J.G. et al. (2016). New insights into the catalytic cleavage of the lignin β‐O‐4 linkage in multifunctional ionic liquid media. Catalysis Science & Technology 6: 1882–1891.

      123 123. Wang, H., Zhang, L., Deng, T. et al. (2016). ZnCl2 induced catalytic conversion of softwood lignin to aromatics and hydrocarbons. Green Chemistry 18: 2802–2810.