The DOI matches its Crossref record; 137 of the 137 references it cites were found in a registry or an index.
Recent advances in the application of deep eutectic solvents as sustainable media as well as catalysts in organic reactions
Open accessAbstract
This review highlights the recent advances using deep eutectic solvents (DESs), deep eutectic ionic liquids (DEILs), low-melting mixtures (LMMs) or low transition temperature mixtures (LTTMs) as green media as well as catalysts in organic reactions.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Room-Temperature Ionic Liquids: Solvents for Synthesis and Catalysis. 2
Hallett, J. P., & Welton, T. (2011) · Chemical Reviews · doi:10.1021/cr1003248 · Cited by 12,578
Deep Eutectic Solvents (DESs) and Their Applications
Smith, E. L., Abbott, A. P., & Ryder, K. S. (2014) · Chemical Reviews · doi:10.1021/cr300162p · Cited by 7,378
Abbott, A. P., Capper, G., Davies, D. L., Rasheed, R. K., & Tambyrajah, V. (2003) · Chemical Communications · doi:10.1039/b210714g · Cited by 5,738
Deep eutectic solvents: syntheses, properties and applications
Zhang, Q., De Oliveira Vigier, K., Royer, S., & Jérôme, F. (2012) · Chemical Society Reviews · doi:10.1039/c2cs35178a · Cited by 4,899
Abbott, A. P., Boothby, D., Capper, G., Davies, D. L., & Rasheed, R. K. (2004) · Journal of the American Chemical Society · doi:10.1021/ja048266j · Cited by 4,340
Natural deep eutectic solvents as new potential media for green technology
Dai, Y., van Spronsen, J., Witkamp, G.-J., Verpoorte, R., & Choi, Y. H. (2013) · Analytica Chimica Acta · doi:10.1016/j.aca.2012.12.019 · Cited by 2,694
Jason, P. H., & Tom, W. (2011) · Chemical Reviews · Cited by 2,270
Low-transition-temperature mixtures (LTTMs): A new generation of designer solvents
Francisco, M., van den Bruinhorst, A., & Kroon, M. C. (2013) · Angewandte Chemie International Edition · doi:10.1002/anie.201207548 · Cited by 1,378
Ionic liquids: a pathway to environmental acceptability
Petkovic, M., Seddon, K. R., Rebelo, L. P. N., & Silva Pereira, C. (2011) · Chem. Soc. Rev. · doi:10.1039/c004968a · Cited by 1,197
Deep Eutectic Solvents: Sustainable Media for Nanoscale and Functional Materials
Wagle, D. V., Zhao, H., & Baker, G. A. (2014) · Accounts of Chemical Research · doi:10.1021/ar5000488 · Cited by 887
Research works printed but not linked: 85
- Liu, 2012, Chem.–Asian. J., 7, 1759, 10.1002/asia.201200289 · doi:10.1002/asia.201200289
- Isambert, 2011, Chem. Soc. Rev., 40, 1347, 10.1039/C0CS00013B · doi:10.1039/c0cs00013b
- Taheri, 2014, ChemSusChem, 7, 2094, 10.1002/cssc.201402220 · doi:10.1002/cssc.201402220
- Taheri, 2014, Green Chem., 16, 3715, 10.1039/C4GC00840E · doi:10.1039/c4gc00840e
- Wang, 2014, Adv. Synth. Catal., 356, 3125, 10.1002/adsc.201400026 · doi:10.1002/adsc.201400026
- Taheri, 2015, Green Chem., 17, 812, 10.1039/C4GC01299B · doi:10.1039/c4gc01299b
- Zhang, 2013, Prog. Chem., 25, 881
- Sebastian, 2014, Electrochim. Acta, 123, 285, 10.1016/j.electacta.2014.01.062 · doi:10.1016/j.electacta.2014.01.062
- Wang, 2014, Prog. Chem., 26, 784
- Li, 2014, Chin. J. Org. Chem., 34, 1074, 10.6023/cjoc201312034 · doi:10.6023/cjoc201312034
- Huang, 2014, RSC Adv., 4, 10188, 10.1039/c3ra46789a · doi:10.1039/c3ra46789a
- Azizi, 2014, Tetrahedron Lett., 55, 1722, 10.1016/j.tetlet.2014.01.104 · doi:10.1016/j.tetlet.2014.01.104
- Yadav, 2014, J. Mol. Liq., 195, 188, 10.1016/j.molliq.2014.02.016 · doi:10.1016/j.molliq.2014.02.016
- Imperato, 2005, Chem. Commun., 1170, 10.1039/B414515A · DOI · Paper page
- Gore, 2012, Adv. Synth. Catal., 354, 2368, 10.1002/adsc.201200257 · doi:10.1002/adsc.201200257
- Zhang, 2008, Ultrason. Sonochem., 15, 673, 10.1016/j.ultsonch.2008.02.008 · doi:10.1016/j.ultsonch.2008.02.008
- Joshi, 2013, Curr. Org. Chem., 17, 2279, 10.2174/13852728113179990040 · doi:10.2174/13852728113179990040
- Stockigt, 2011, Angew. Chem., Int. Ed., 50, 8538, 10.1002/anie.201008071 · doi:10.1002/anie.201008071
- Tummatorn, 2014, RSC Adv., 4, 20048, 10.1039/C4RA02158D · doi:10.1039/c4ra02158d
- Porcheddu, 2012, Org. Lett., 14, 6112, 10.1021/ol3030956 · doi:10.1021/ol3030956
- Siddalingamurthy, 2013, Tetrahedron Lett., 54, 5591, 10.1016/j.tetlet.2013.07.157 · doi:10.1016/j.tetlet.2013.07.157
- Gore, 2012, Org. Lett., 14, 4568, 10.1021/ol302034r · doi:10.1021/ol302034r
- More, 2014, Catal. Lett., 144, 1393, 10.1007/s10562-014-1288-3 · doi:10.1007/s10562-014-1288-3
- Ma, 2013, Appl. Catal., A, 457, 34, 10.1016/j.apcata.2013.03.005 · doi:10.1016/j.apcata.2013.03.005
- Zuo, 2009, J. Chem. Res., 14, 10.3184/030823409X393628 · doi:10.3184/030823409x393628
- Deng, 2012, Appl. Organomet. Chem., 26, 164, 10.1002/aoc.1864 · doi:10.1002/aoc.1864
- Silveira, 2012, Curr. Org. Chem., 16, 1540, 10.2174/138527212800672538 · doi:10.2174/138527212800672538
- Akbaslar, 2014, Synth. Commun., 44, 1323, 10.1080/00397911.2013.857691 · doi:10.1080/00397911.2013.857691
- Liu, 2009, Tetrahedron Lett., 50, 916, 10.1016/j.tetlet.2008.12.022 · doi:10.1016/j.tetlet.2008.12.022
- Zhang, 2007, Synth. Commun., 37, 209, 10.1080/00397910601031652 · doi:10.1080/00397910601031652
- Bartoli, 2010, Chem. Soc. Rev., 39, 4449, 10.1039/b923063g · doi:10.1039/b923063g
- Shiri, 2012, Chem. Rev., 112, 3508, 10.1021/cr2003954 · doi:10.1021/cr2003954
- Dalpozzo, 2015, Chem. Soc. Rev., 44, 742, 10.1039/C4CS00209A · doi:10.1039/c4cs00209a
- Mo, 2005, Synth. Commun., 35, 1997, 10.1081/SCC-200066653 · doi:10.1081/scc-200066653
- Mulla, 2012, RSC Adv., 2, 3525, 10.1039/c2ra00849a · doi:10.1039/c2ra00849a
- Liang, 2014, Catal. Commun., 55, 11, 10.1016/j.catcom.2014.06.005 · doi:10.1016/j.catcom.2014.06.005
- Jella, 2013, Tetrahedron, 69, 10249, 10.1016/j.tet.2013.10.037 · doi:10.1016/j.tet.2013.10.037
- Gu, 2012, Green Chem., 14, 2091, 10.1039/c2gc35635j · DOI · Paper page
- Guo, 2013, Tetrahedron, 69, 9931, 10.1016/j.tet.2013.09.082 · doi:10.1016/j.tet.2013.09.082
- Li, 2015, RSC Adv., 5, 25625, 10.1039/C5RA01677K · doi:10.1039/c5ra01677k
- Li, 2014, Adv. Synth. Catal., 356, 537, 10.1002/adsc.201300790 · doi:10.1002/adsc.201300790
- Keglevich, 2012, Molecules, 17, 12821, 10.3390/molecules171112821 · doi:10.3390/molecules171112821
- Sun, 2010, J. Chin. Chem. Soc., 57, 1315, 10.1002/jccs.201000194 · doi:10.1002/jccs.201000194
- Hou, 2011, Appl. Organomet. Chem., 25, 47, 10.1002/aoc.1687 · doi:10.1002/aoc.1687
- Sobhani, 2014, RSC Adv., 4, 15797, 10.1039/c4ra01124d · doi:10.1039/c4ra01124d
- Arrayas, 2009, Chem. Soc. Rev., 38, 1940, 10.1039/b820303b · doi:10.1039/b820303b
- Karimi, 2013, Synthesis, 45, 2769, 10.1055/s-0033-1339479 · doi:10.1055/s-0033-1339479
- Brauch, 2013, Chem. Soc. Rev., 42, 4948, 10.1039/c3cs35505e · doi:10.1039/c3cs35505e
- Azizi, 2014, Synlett, 25, 1085, 10.1055/s-0033-1341050 · doi:10.1055/s-0033-1341050
- Khedkar, 2014, Mini-Rev. Med. Chem., 14, 282, 10.2174/1389557513666131119204126 · doi:10.2174/1389557513666131119204126
- Wang, 2014, Green Process. Synth., 3, 457, 10.1515/gps-2014-0056 · doi:10.1515/gps-2014-0056
- Sun, 2010, Synth. Commun., 40, 587, 10.1080/00397910903007079 · doi:10.1080/00397910903007079
- Guo, 2013, ACS Comb. Sci., 15, 557, 10.1021/co400107j · doi:10.1021/co400107j
- Chaskar, 2014, Lett. Org. Chem., 11, 480, 10.2174/1570178611666140210213413 · doi:10.2174/1570178611666140210213413
- Deng, 2012, ACS Comb. Sci., 14, 335, 10.1021/co3000264 · doi:10.1021/co3000264
- Guo, 2013, Tetrahedron, 69, 2056, 10.1016/j.tet.2012.12.081 · DOI
- Khandelwal, 2014, Comb. Chem. High Throughput Screening, 17, 763, 10.2174/1386207317666141016125218 · doi:10.2174/1386207317666141016125218
- Yan, 2015, Chin. J. Org. Chem., 35, 384, 10.6023/cjoc201409028 · doi:10.6023/cjoc201409028
- Wang, 2010, Monatsh. Chem., 141, 425, 10.1007/s00706-010-0283-7 · doi:10.1007/s00706-010-0283-7
- Zhao, 2014, RSC Adv., 4, 51089, 10.1039/C4RA09984B · doi:10.1039/c4ra09984b
- Aziizi, 2014, J. Mol. Liq., 196, 153, 10.1016/j.molliq.2014.03.013 · doi:10.1016/j.molliq.2014.03.013
- Azizi, 2012, Sci. World J., 908702
- Li, 2014, New J. Chem., 38, 2435, 10.1039/c3nj01368e · doi:10.1039/c3nj01368e
- Maiti, 2010, J. Org. Chem., 75, 1674, 10.1021/jo902661y · doi:10.1021/jo902661y
- Atar, 2013, Tetrahedron Lett., 54, 5624, 10.1016/j.tetlet.2013.08.016 · doi:10.1016/j.tetlet.2013.08.016
- Bharate, 2013, RSC Adv., 3, 21736, 10.1039/c3ra43324b · doi:10.1039/c3ra43324b
- Siddalingamurthy, 2013, Synth. Commun., 43, 3153, 10.1080/00397911.2013.769601 · doi:10.1080/00397911.2013.769601
- Harishkumar, 2011, Org. Commun., 4, 26
- Lu, 2009, Appl. Organomet. Chem., 23, 165, 10.1002/aoc.1488 · doi:10.1002/aoc.1488
- Mahajan, 2014, Org. Prep. Proced. Int., 46, 463, 10.1080/00304948.2014.944408 · doi:10.1080/00304948.2014.944408
- Azizi, 2015, J. Mol. Liq., 206, 268, 10.1016/j.molliq.2015.02.033 · doi:10.1016/j.molliq.2015.02.033
- Azizi, 2015, Monatsh. Chem., 146, 10.1007/s00706-015-1447-2 · doi:10.1007/s00706-015-1447-2
- Singh, 2014, Tetrahedron Lett., 55, 7243, 10.1016/j.tetlet.2014.11.053 · doi:10.1016/j.tetlet.2014.11.053
- Azizi, 2012, C. R. Chim., 15, 768, 10.1016/j.crci.2012.06.011 · doi:10.1016/j.crci.2012.06.011
- Azizi, 2014, Ind. Eng. Chem. Res., 53, 15561, 10.1021/ie502019z · doi:10.1021/ie502019z
- Sanchez, 2008, Synlett, 1101, 10.1055/s-2008-1066990 · doi:10.1055/s-2008-1066990
- Liu, 2008, Synthesis, 3314
- Liu, 2012, Adv. Synth. Catal., 354, 441, 10.1002/adsc.201100561 · doi:10.1002/adsc.201100561
- Li, 2013, Adv. Synth. Catal., 355, 2952, 10.1002/adsc.201300551 · doi:10.1002/adsc.201300551
- Dai, 2014, J. Chem. Res., 38, 183, 10.3184/174751914X13923144871332 · doi:10.3184/174751914x13923144871332
- Wang, 2014, J. Fluorine Chem., 158, 44, 10.1016/j.jfluchem.2013.12.006 · doi:10.1016/j.jfluchem.2013.12.006
- Deng, 2011, Green Chem., 13, 2576, 10.1039/c1gc15470b · doi:10.1039/c1gc15470b
- Zhao, 2014, Appl. Organomet. Chem., 28, 635, 10.1002/aoc.3173 · doi:10.1002/aoc.3173
- Ruß, 2012, Synth. Commun., 42, 3112, 10.1080/00397911.2011.576375 · doi:10.1080/00397911.2011.576375
- Pöehnlein, 2015, Eur. J. Lipid Sci. Technol., 117, 161, 10.1002/ejlt.201400459 · doi:10.1002/ejlt.201400459
Cited by
Natural deep eutectic solvents: Properties, applications, and perspectives
Liu, Y., Friesen, J. B., McAlpine, J. B., Lankin, D. C., Chen, S.-N., & Pauli, G. F. (2018) · Journal of Natural Products · doi:10.1021/acs.jnatprod.7b00945 · Cited by 1,304
Ruesgas-Ramón, M., Figueroa-Espinoza, M. C., & Durand, E. (2017) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.7b01054 · Cited by 790
Deep Eutectic Solvents: The Organic Reaction Medium of the Century
Alonso, D. A., Baeza, A., Chinchilla, R., Guillena, G., Pastor, I. M., & Ramón, D. J. (2016) · European Journal of Organic Chemistry · doi:10.1002/ejoc.201501197 · Cited by 709
Application of deep eutectic solvents in analytical chemistry. A review
Shishov, A., Bulatov, A., Locatelli, M., Carradori, S., & Andruch, V. (2017) · Microchemical Journal · doi:10.1016/j.microc.2017.07.015 · Cited by 561
Abranches, D. O., Martins, M. A. R., Silva, L. P., Schaeffer, N., Pinho, S. P., & Coutinho, J. A. P. (2019) · Chemical Communications · doi:10.1039/c9cc04846d · Cited by 550
Metadata
- Authors
- Liu, P., Hao, J.-W., Mo, L.-P., & Zhang, Z.-H.
- Venue
- RSC Advances
- Publisher
- Royal Society of Chemistry (RSC)
- Published
- 2015
- Volume
- 5
- Issue
- 60
- Pages
- 48675-48704
- ISSN
- 2046-2069 (ISSN-L)
- OpenAlex
- W1776656534
- Cited by
- 663
- References
- 137
- FWCI
- 18.90
- Type
- journal article
- Language
- en
- Open access
- bronze
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Recent advances in the application of deep eutectic solvents as sustainable media as well as catalysts in organic reactions. https://app.cochat.ai/papers/10.1039/c5ra05746a
- The paper
- Liu, P., Hao, J.-W., Mo, L.-P., & Zhang, Z.-H. (2015). Recent advances in the application of deep eutectic solvents as sustainable media as well as catalysts in organic reactions. RSC Advances. https://doi.org/10.1039/c5ra05746a
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.