Open Access
Review
Issue
OCL
Volume 22, Number 4, July-August 2015
Article Number D408
Number of page(s) 6
Section Dossier: 12th Euro Fed Lipids Congress: Oils, Fats and Lipids: From Lipidomics to Industrial Innovation
DOI https://doi.org/10.1051/ocl/2015026
Published online 07 July 2015
  • Abbott AP, Boothby D, Capper G, Davies DL, Rasheed RK. 2004. Deep Eutectic Solvents formed between choline chloride and carboxylic acids: Versatile alternatives to ionic liquids. J. Am. Chem. Soc. 126: 9142–9147. [CrossRef] [PubMed] [Google Scholar]
  • Abbott AP, Capper G, Davies DL, Rasheed RK, Tambyrajah V. 2003. Novel solvent properties of choline chloride/urea mixtures. Chem. Commun. 70–71. [Google Scholar]
  • Alemán M, Bou R, Guardiola F, et al. 2015. Antioxidative effect of lipophilized caffeic acid in fish oil enriched mayonnaise and milk. Food Chem. 167: 236–244. [CrossRef] [PubMed] [Google Scholar]
  • Borse BN, Shukla SR, Sonawane YA, Shankerling GS. 2013. Synthesis of some novel pyrimidinedione and pyrimidinetrione derivatives by a greener method: Study of their antimicrobial activity and photophysical properties. Synth. Commun. 43: 865–876. [CrossRef] [Google Scholar]
  • Choi YH, van Spronsen J, Dai Y, et al. 2011. Are natural deep eutectic solvents the missing link in understanding cellular metabolism and physiology? Plant Physiol. 156: 1701–1705. [CrossRef] [PubMed] [Google Scholar]
  • Dai Y, van Spronsen J, Witkamp GJ, Verpoorte R, Choi YH. 2013. Natural deep eutectic solvents as new potential media for green technology. Anal. Chim. Acta 766: 61–68. [CrossRef] [PubMed] [Google Scholar]
  • Durand E, Lecomte J, Baréa B, et al. 2012. Evaluation of deep eutectic solvents as new media for Candida antarctica B lipase catalyzed reactions. Process Biochem. 47: 2081–2089. [CrossRef] [Google Scholar]
  • Durand E, Lecomte J, Baréa B, et al. 2013. Evaluation of deep eutectic solvent–water binary mixtures for lipase-catalyzed lipophilization of phenolic acids. Green Chem. 15: 2275. [CrossRef] [Google Scholar]
  • Durand E, Lecomte J, Villeneuve P. 2013. Deep eutectic solvents: Synthesis, application, and focus on lipase-catalyzed reactions. Eur. J. Lipid Sci. Technol. 115: 379–385. [CrossRef] [Google Scholar]
  • Durand E, Lecomte J, Baréa B, et al. 2014. Towards a better understanding of how to improve lipase-catalyzed reactions using deep eutectic solvents based on choline chloride. Eur. J. Lipid Sci. Technol. 116: 16–23. [CrossRef] [Google Scholar]
  • Durand E, Bayrasy C, Laguerre M, et al. 2015. Regioselective synthesis of diacylglycerol rosmarinates and evaluation of their antioxidant activity in fibroblasts. Eur. J. Lipid Sci. Technol., in press. [Google Scholar]
  • Figueroa-Espinoza MC, Villeneuve P. 2005. Phenolic acids enzymatic lipophilization. J. Agric. Food Chem. 53: 2779–2787. [Google Scholar]
  • Gorke JT, Srienc F, Kazlauskas RJ. 2008. Hydrolase-catalyzed biotransformations in deep eutectic solvents. Chem. Commun. 1235–1237. [Google Scholar]
  • Gorke JT, Kazlauskas RJ. 2009. Enzymatic processing in deep eutectic solvents. US PATENT, N° 20090117. [Google Scholar]
  • Huang WY, Cai YZ, Zhang Y. 2009. Natural phenolic compounds from medicinal herbs and dietary plants: potential use for cancer prevention. Nutr. Cancer 62: 1–20. [CrossRef] [Google Scholar]
  • Kareem MA, Mjalli FS, Hashim MA, Alnashef IM. 2010. Phosphonium-based ionic liquids analogues and their physical properties. J. Chem. Eng. Data 55: 4632–4637. [CrossRef] [Google Scholar]
  • Laguerre M, López Giraldo LJ, Lecomte J, et al. 2010. Relationship between hydrophobicity and antioxidant ability of “phenolipids” in emulsion: A parabolic effect of the chain length of rosmarinate esters. J. Agric. Food Chem. 58: 2869–2876. [Google Scholar]
  • Li W, Zhang Z, Han B, et al. 2008. Switching the basicity of ionic liquids by CO2. Green Chem. 10: 1142–1145. [CrossRef] [Google Scholar]
  • Lindberg D, de la Fuente Revenga M, Widersten M. 2010. Deep eutectic solvents (DESs) are viable cosolvents for enzyme-catalyzed epoxide hydrolysis. J. Biotechnol. 147: 169–171. [CrossRef] [PubMed] [Google Scholar]
  • Maugeri Z, Domínguez de María P. 2012. Novel choline-chloride-based deep-eutectic-solvents with renewable hydrogen bond donors: levulinic acid and sugar-based polyols. RSC Adv. 2: 421. [CrossRef] [Google Scholar]
  • Maugeri Z, Leitner W, Domínguez De María P. 2013. Chymotrypsin-catalyzed peptide synthesis in deep eutectic solvents. Eur. J. Organic Chem. 4223–4228. [Google Scholar]
  • Monhemi H, Housaindokht MR, Moosavi-Movahedi AA, Bozorgmehr MR. 2014. How a protein can remain stable in a solvent with high content of urea: insights from molecular dynamics simulation of Candida antarctica lipase B in urea: choline chloride deep eutectic solvent. Phys. Chem. Chem. Phys. 16: 14882–93. [CrossRef] [PubMed] [Google Scholar]
  • Nam MW, Zhao J, Lee MS, Jeong JH, Lee J. 2015. Enhanced extraction of bioactive natural products using tailor-made deep eutectic solvents: application to flavonoid extraction from Flos sophorae. Green Chem. 17: 1718–1727. [CrossRef] [Google Scholar]
  • Pang N, Gu SS, Wang J, et al. 2013. A novel chemoenzymatic synthesis of propyl caffeate using lipase-catalyzed transesterification in ionic liquid. Bioresour. Technol. 139: 337–342. [CrossRef] [PubMed] [Google Scholar]
  • Ranke J, Mölter K, Stock F, et al. 2004. Biological effects of imidazolium ionic liquids with varying chain lengths in acute Vibrio fischeri and WST-1 cell viability assays. Ecotoxicol. Environ. Saf. 58: 396–404. [CrossRef] [PubMed] [Google Scholar]
  • Soobrattee MA, Neergheen VS, Luximon-Ramma A, Aruoma OI, Bahorun T. 2005. Phenolics as potential antioxidant therapeutic agents: Mechanism and actions. Mutat. Res.-Fund. Mol. Mech. Mutagen. 579: 200–213. [Google Scholar]
  • Stolte S, Arning J, Bottin-Weber U, et al. 2006. Anion effects on the cytotoxicity of ionic liquids. Green Chem. 8: 621-629. [CrossRef] [Google Scholar]
  • Su WC, Wong DSH, Li MH. 2009. Effect of Water on Solubility of Carbon Dioxide in (Aminomethanamide + 2-Hydroxy- N, N, N-trimethylethanaminium Chloride). J. Chem. Eng. Data 54: 1951–1955. [CrossRef] [Google Scholar]
  • Van den Berghe W. 2012. Epigenetic impact of dietary polyphenols in cancer chemoprevention: Lifelong remodeling of our epigenomes. Pharmacol. Res. 65: 565–576. [CrossRef] [PubMed] [Google Scholar]
  • Villeneuve P. 2007. Lipases in lipophilization reactions. Biotechnol. Adv. 25: 515-536. [CrossRef] [PubMed] [Google Scholar]
  • Weitkamp P, Vosmann K, Weber N. 2006. Highly efficient preparation of lipophilic hydroxycinnamates by solvent-free lipase-catalyzed transesterification. J. Agric. Food Chem. 54: 7062–7068. [CrossRef] [PubMed] [Google Scholar]
  • Wu BP, Wen Q, Xu H, Yang Z. 2014. Insights into the impact of deep eutectic solvents on horseradish peroxidase: Activity, stability and structure. J. Mol. Catal. B. Enzymatic 101: 101–107. [CrossRef] [Google Scholar]
  • Yang Z, Guo Z, Xu X. 2012. Enzymatic lipophilisation of phenolic acids through esterification with fatty alcohols in organic solvents. Food Chem. 132: 1311–1315. [CrossRef] [Google Scholar]
  • Zhao H, Baker GA, Holmes S. 2011. Protease activation in glycerol-based deep eutectic solvents. J. Mol. Catal. B Enzymatic 72: 163–167. [CrossRef] [Google Scholar]
  • Zhao H, Zhang C, Crittle TD. 2013. Choline-based deep eutectic solvents for enzymatic preparation of biodiesel from soybean oil. J. Mol. Catal. B Enzymatic 85-86: 243–247. [CrossRef] [Google Scholar]

Current usage metrics show cumulative count of Article Views (full-text article views including HTML views, PDF and ePub downloads, according to the available data) and Abstracts Views on Vision4Press platform.

Data correspond to usage on the plateform after 2015. The current usage metrics is available 48-96 hours after online publication and is updated daily on week days.

Initial download of the metrics may take a while.