The DOI matches its Crossref record; 105 of the 105 references it cites were found in a registry or an index.
Polyethylene glycol: A promising approach for sustainable organic synthesis
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Polyethylene glycol has the potential to substitute classical solvents due to its low toxicity to humans and the environment [72].”
From Use of green alternative solvents in dispersive liquid‐liquid microextraction: A review (2022) · cites this paper as [72]
Citations
Cites
Maeda, H. (2001) · Advances in Enzyme Regulation · doi:10.1016/s0065-2571(00)00013-3 · Cited by 2,495
Polyethylene glycol and solutions of polyethylene glycol as green reaction media
Ra, J. C. A. K. L. O., Spear, S. K., Huddleston, J. G., & Rogers, R. D. (2005) · Green Chemistry · doi:10.1039/b413546f · Cited by 1,039
Chemically recyclable polymers: a circular economy approach to sustainability
Hong, M., & Chen, E. Y.-X. (2017) · Green Chemistry · doi:10.1039/c7gc01496a · Cited by 876
Bailey, F. E., & Koleske, J. (1976) · Cited by 551
Maleki, A. R. (2017) · Ultrasonics Sonochemistry · doi:10.1016/j.ultsonch.2017.07.020 · Cited by 281
Maleki, A. R. (2012) · Tetrahedron · doi:10.1016/j.tet.2012.07.034 · Cited by 270
Heldebrant, D. J., & Jessop, P. G. (2003) · Journal of the American Chemical Society · doi:10.1021/ja029131l · Cited by 242
Canadian Environmental Protection Act
(1989) · Umweltwissenschaften und Schadstoff-Forschung · doi:10.1007/bf02937017 · Cited by 242
Maleki, A. R. (2013) · Tetrahedron Letters · doi:10.1016/j.tetlet.2013.01.123 · Cited by 229
Li, W.-D., & Ding, E. (2007) · Solar Energy Materials and Solar Cells · doi:10.1016/j.solmat.2007.01.011 · Cited by 188
Polyethylene glycol (PEG) as a green solvent for carbon–carbon bond formation reactions
Vafaeezadeh, M., & Hashemi, M. M. (2015) · Journal of Molecular Liquids · doi:10.1016/j.molliq.2015.03.003 · Cited by 130
Polyethyleneglycol as scaffold and solvent for reusable C C coupling homogeneous Pd catalysts
Corma, A., Garcı́a, H., & Leyva‐Pérez, A. (2006) · Journal of Catalysis · doi:10.1016/j.jcat.2006.03.007 · Cited by 124
Jain, S. L., Singhal, S., & Sain, B. (2007) · Green Chemistry · doi:10.1039/b702311a · Cited by 119
Hou, Z., Theyssen, N., & Leitner, W. (2006) · Green Chemistry · doi:10.1039/b606740a · Cited by 118
Polyethylene glycol as a promising synthetic material for repair of spinal cord injury
Chen, X., Tu, Y., Sun, S.-Z., Kong, X., Tang, Q.-Y., & Sun, Z. (2017) · Neural Regeneration Research · doi:10.4103/1673-5374.208597 · Cited by 113
Corma, A., Garcı́a, H., & Leyva‐Pérez, A. (2005) · Tetrahedron · doi:10.1016/j.tet.2005.06.119 · Cited by 106
Sharma, U. K., Kumar, N., Verma, P. K., Kumar, V., & Singh, B. (2012) · Green Chemistry · doi:10.1039/c2gc35452g · Cited by 103
PS–PEG–SO3H as an efficient catalyst for 3,4-dihydropyrimidones via Biginelli reaction
Quan, Z., Da, Y., Zhang, Z., & Wang, X. (2008) · Catalysis Communications · doi:10.1016/j.catcom.2008.12.017 · Cited by 103
Xavier, V. A. R. J., Bharathiraja, B., Badathala, V., Arokiyaraj, S., Iyyappan, J., & Kumar, R. P. (2019) · Bioresource Technology · doi:10.1016/j.biortech.2019.03.030 · Cited by 93
Mirfakhraei, S., Hekmati, M., Eshbala, F. H., & Veisi, H. (2017) · New Journal of Chemistry · doi:10.1039/c7nj02513k · Cited by 89
She, J., Jiang, Z. R., & Wang, Y. (2008) · Tetrahedron Letters · doi:10.1016/j.tetlet.2008.11.082 · Cited by 86
Yedage, S. L., & Bhanage, B. M. (2016) · Green Chemistry · doi:10.1039/c6gc01581f · Cited by 86
Zhao, H. L., Zhang, T., Yan, T., & Cai, M. (2015) · The Journal of Organic Chemistry · doi:10.1021/acs.joc.5b01388 · Cited by 81
Chandrasekhar, S., Prakash, S. J., & Chennamaneni, L. R. (2006) · The Journal of Organic Chemistry · doi:10.1021/jo052604x · Cited by 80
Polyethylene glycols as soluble, recoverable, phase-transfer catalysts
Harris, J. M., Hundley, N. H., Shannon, T. G., & Struck, E. C. (1982) · The Journal of Organic Chemistry · doi:10.1021/jo00145a041 · Cited by 76
Wang, X., Quan, Z., Wang, F., Wang, M., Zhang, Z., & Li, Z. (2006) · Synthetic Communications · doi:10.1080/00397910500383519 · Cited by 75
Zhao, H. L., Cheng, M., Zhang, J., & Cai, M. (2013) · Green Chemistry · doi:10.1039/c3gc42278j · Cited by 74
Systematic review and meta analysis: polyethylene glycol in adults with non-organic constipation
Belsey, J., Geraint, M., & Dixon, T. A. (2010) · International Journal of Clinical Practice · doi:10.1111/j.1742-1241.2010.02397.x · Cited by 70
Karnakar, K., Murthy, S. N., Ramesh, K., Satish, G., Nanubolu, J. B., & Nageswar, Y. V. D. (2012) · Tetrahedron Letters · doi:10.1016/j.tetlet.2012.03.135 · Cited by 70
Aerobic and anaerobic biodegradation of polyethylene glycols using sludge microbes
Huang, Y., Li, Q., Deng, X. H., Lu, Y., Liao, X., Hong, M.-Y., & Wang, Y. (2004) · Process Biochemistry · doi:10.1016/j.procbio.2003.12.004 · Cited by 69
Ramesh, R., & Lalitha, A. (2015) · RSC Advances · doi:10.1039/c5ra07726e · Cited by 67
Maleki, A. R., Azizi, M., & Emdadi, Z. (2018) · Green Chemistry Letters and Reviews · doi:10.1080/17518253.2018.1547795 · Cited by 62
Nagaraju, A., Ramulu, B. J., Shukla, G., Srivastava, A., Verma, G. K., Raghuvanshi, K., & Singh, M. S. (2014) · Green Chemistry · doi:10.1039/c4gc01431f · Cited by 60
Hiebel, M., Fall, Y., Scherrmann, M., & Berteina‐Raboin, S. (2014) · European Journal of Organic Chemistry · doi:10.1002/ejoc.201402079 · Cited by 56
Nagarapu, L., Mallepalli, R., Lingappa, Y., & Bantu, R. (2011) · Tetrahedron Letters · doi:10.1016/j.tetlet.2011.04.095 · Cited by 56
Tiwari, A. R., & Bhanage, B. M. (2015) · Green Chemistry · doi:10.1039/c5gc01884f · Cited by 55
Rostami, A., Rostami, A., Iranpoor, N., & Zolfigol, M. A. (2015) · Tetrahedron Letters · doi:10.1016/j.tetlet.2015.11.093 · Cited by 55
Maleki, A. R., Zand, P., & Mohseni, Z. (2016) · RSC Advances · doi:10.1039/c6ra24029a · Cited by 55
Chary, R. G., Reddy, G. R., Ganesh, Y. S. S., Prasad, K. V., Raghunadh, A., Krishna, T., Mukherjee, S., & Pal, M. (2014) · Advanced Synthesis & Catalysis · doi:10.1002/adsc.201300712 · Cited by 53
Shekouhy, M. (2012) · Catalysis Science & Technology · doi:10.1039/c2cy00493c · Cited by 52
Simple and efficient CuI/PEG-400 system for amination of aryl halides with aqueous ammonia
Chen, J., Yuan, T., Hao, W., & Cai, M. (2011) · Tetrahedron Letters · doi:10.1016/j.tetlet.2011.02.096 · Cited by 52
Poly(ethylene Glycol) and Derivatives as Phase Transfer Catalysts
Totten, G. E., & Clinton, N. A. (1998) · Journal of macromolecular science. Part C, Reviews in macromolecular chemistry and physics/Journal of macromolecular science. Reviews in macromolecular chemistry and physics · doi:10.1080/15583729808545778 · Cited by 50
Feu, K. S., de la Torre, A. F., Silva, S., de Moraes, M. A. F., Corrêa, A. G., & Paixão, M. W. (2014) · Green Chemistry · doi:10.1039/c4gc00098f · Cited by 49
Hasaninejad, A., & Beyrati, M. (2018) · RSC Advances · doi:10.1039/c7ra13133j · Cited by 49
An atom transfer radical polymerization system: catalyzed by an iron catalyst in PEG-400
Ding, M., Jiang, X., Peng, J., Zhang, L., Cheng, Z., & Zhu, X. (2014) · Green Chemistry · doi:10.1039/c4gc01169d · Cited by 47
Vekariya, R. H., & Patel, H. D. (2015) · RSC Advances · doi:10.1039/c5ra06532a · Cited by 46
A Microwave‐Assisted Heck Reaction in Poly(ethylene glycol) for the Synthesis of Benzazepines
Declerck, V., Ribière, P., Nédellec, Y., Allouchi, H., Martínez, J., & Lamaty, F. (2006) · European Journal of Organic Chemistry · doi:10.1002/ejoc.200600680 · Cited by 45
Zhu, D., Chen, J., Xiao, H., Liu, M., Ding, J., & Wu, H. (2009) · Synthetic Communications · doi:10.1080/00397910802691874 · Cited by 44
Paul, S., & Das, A. R. (2012) · Catalysis Science & Technology · doi:10.1039/c2cy20117h · Cited by 43
Kumar, P., Dehiya, B. S., & Sindhu, A. (2019) · Ceramics International · doi:10.1016/j.ceramint.2019.01.145 · Cited by 42
Rostami, A., Rostami, A., Ghaderi, A., & Zolfigol, M. A. (2015) · RSC Advances · doi:10.1039/c5ra05244k · Cited by 41
Visible light-driven organic form-stable phase change materials for solar energy storage
Wang, Y., Tang, B., & Zhang, S. (2012) · RSC Advances · doi:10.1039/c2ra20904g · Cited by 40
Sauvagnat, B., Lamaty, F., Lazaro, R., & Martínez, J. (1998) · Tetrahedron Letters · doi:10.1016/s0040-4039(97)10722-5 · Cited by 39
Mascitti, A., Lupacchini, M., Guerra, R., Taydakov, I. V., Tonucci, L., d’Alessandro, N., Lamaty, F., Martínez, J., & Colacino, E. (2017) · Beilstein Journal of Organic Chemistry · doi:10.3762/bjoc.13.3 · Cited by 39
Wang, X., Quan, Z., & Zhang, Z. (2007) · Tetrahedron · doi:10.1016/j.tet.2007.05.108 · Cited by 38
Zhong, X., Dou, G., & Wang, D. (2013) · Molecules · doi:10.3390/molecules181113139 · Cited by 36
The Role of PEG on Pd- and Cu-Catalyzed Cross-Coupling Reactions
Pires, M. J. D., Purificação, S. I., Santos, A. S., & Marques, M. M. B. (2017) · Synthesis · doi:10.1055/s-0036-1589498 · Cited by 36
Chary, R. G., Reddy, G. R., Ganesh, Y. S. S., Prasad, K. V., Chandra, S. K. P., Mukherjee, S., & Pal, M. (2013) · RSC Advances · doi:10.1039/c3ra40969d · Cited by 35
Balwe, S. G., Lim, K. T., Cho, B. G., & Jeong, Y. T. (2017) · Tetrahedron · doi:10.1016/j.tet.2017.05.047 · Cited by 35
FeF 3 -catalyzed MCR in PEG-400: ultrasound assisted synthesis of N-substituted 2-aminopyridines
Reddy, D. N. K., Chandrasekhar, K. B., Ganesh, Y. S. S., Reddy, G. R., Kumar, J., Kapavarapu, R., & Pal, M. (2016) · RSC Advances · doi:10.1039/c6ra14228a · Cited by 34
Khan, M. N., Karamthulla, S., Choudhury, L. H., & Faizi, M. S. H. (2015) · RSC Advances · doi:10.1039/c5ra02403j · Cited by 33
Reddy, M. V., Kim, J. S., Lim, K. T., & Jeong, Y. T. (2014) · Tetrahedron Letters · doi:10.1016/j.tetlet.2014.09.135 · Cited by 33
Qu, X., Sun, P., Li, T., & Mao, J. (2011) · Advanced Synthesis & Catalysis · doi:10.1002/adsc.201100008 · Cited by 33
PEG-SO3H: A mild and efficient recyclable catalyst for the synthesis of coumarin derivatives
Nazeruddin, G. M., Pandharpatte, M. S., & Mulani, K. (2011) · Comptes Rendus Chimie · doi:10.1016/j.crci.2011.10.005 · Cited by 31
Siddiqui, Z. N., & Khan, T. (2013) · RSC Advances · doi:10.1039/c3ra44685a · Cited by 30
Chandrasekhar, S., Patro, V., Reddy, G. P., & Gree, R. L. (2012) · Tetrahedron Letters · doi:10.1016/j.tetlet.2012.09.008 · Cited by 29
Heirati, S. Z. D., Shirini, F., & Shojaeı, A. F. (2016) · RSC Advances · doi:10.1039/c6ra11201c · Cited by 28
Safaei‐Ghomi, J., & Eshteghal, F. (2017) · Ultrasonics Sonochemistry · doi:10.1016/j.ultsonch.2017.03.047 · Cited by 28
Li, X., Yuan, T., Yu, Y., & Chen, J. (2014) · Tetrahedron · doi:10.1016/j.tet.2014.10.075 · Cited by 28
Billault, I., Pessel, F., Petit, A., Turgis, R., & Scherrmann, M. (2015) · New Journal of Chemistry · doi:10.1039/c4nj01784f · Cited by 27
Paul, S., Ghosh, S., Bhattacharyya, P., & Das, A. R. (2013) · RSC Advances · doi:10.1039/c3ra42352b · Cited by 25
Azizi, M., Maleki, A. R., Hakimpoor, F., Firouzi‐Haji, R., Ghassemi, M., & Rahimi, J. (2018) · Letters in Organic Chemistry · doi:10.2174/1570178615666180126155204 · Cited by 25
Maleki, A. R., Zand, P., Mohseni, Z., & Firouzi‐Haji, R. (2018) · Nano-Structures & Nano-Objects · doi:10.1016/j.nanoso.2018.03.012 · Cited by 24
Reusable Pd@PEG Catalyst for Aerobic Dehydrogenative C−H/C−H Arylations of 1,2,3‐Triazoles
Ferlin, F., Yetra, S. R., Warratz, S., Vaccaro, L., & Ackermann, L. (2019) · Chemistry - A European Journal · doi:10.1002/chem.201902901 · Cited by 24
Prasad, D., & Nath, M. (2011) · Catalysis Science & Technology · doi:10.1039/c1cy00407g · Cited by 23
Lei, J., He, H.-Y., Huang, J. L., Wu, Q., Yuan, M., Fu, H., Zheng, X., Chen, H., & Li, R.-X. (2017) · RSC Advances · doi:10.1039/c7ra02638b · Cited by 20
Siddaiah, V., Basha, G. M., Rao, G. P., Prasad, U. V., & Rao, R. S. (2011) · Synthetic Communications · doi:10.1080/00397911.2010.528289 · Cited by 19
Rao, M. S., Haritha, M., Chandrasekhar, N., Rao, M. V. B., & Pal, M. (2014) · Tetrahedron Letters · doi:10.1016/j.tetlet.2014.01.115 · Cited by 19
Siddaiah, V., Basha, G. M., Tadikonda, R., Nakka, M., Sudhakar, D., Yadav, S. K., & Voosala, C. (2014) · Tetrahedron Letters · doi:10.1016/j.tetlet.2014.03.040 · Cited by 18
Potassium carbonate as a green catalyst for Markovnikov addition of azoles to vinyl acetate in PEG
Kidwai, M., Lal, M., Mishra, N. K., & Jahan, A. (2012) · Green Chemistry Letters and Reviews · doi:10.1080/17518253.2012.704082 · Cited by 17
Kiasat, A. R., & Mehrjardi, M. F. (2008) · Synthetic Communications · doi:10.1080/00397910802044231 · Cited by 16
Mekala, R., Balam, S. K., Harinath, J. P. S., Gajjal, R. R., & Cirandur, S. R. (2015) · Cogent Chemistry · doi:10.1080/23312009.2015.1049932 · Cited by 16
A one-pot direct regioselective iodination of Fischer-Borsche product using periodic acid in PEG-400
Ghom, M. H., Naykode, M. S., Humne, V. T., & Lokhande, P. D. (2019) · Tetrahedron Letters · doi:10.1016/j.tetlet.2019.03.022 · Cited by 15
Reddy, D. N. K., Chandrasekhar, K. B., Ganesh, Y. S. S., Gorantla, S. S., Ramanjaneyulu, S., Kumar, K. S., & Pal, M. (2014) · Synthetic Communications · doi:10.1080/00397911.2014.966392 · Cited by 13
Kasaboina, S., Bollu, R., Gomedhika, P. M., Venkatesh, R., Nagarapu, L., Dumala, N., Grover, P., & Nanubolu, J. B. (2018) · Tetrahedron Letters · doi:10.1016/j.tetlet.2018.06.068 · Cited by 13
Zolfigol, M. A., Ghaemi, E., Madrakian, E., & Niknam, K. (2008) · Journal of the Chinese Chemical Society · doi:10.1002/jccs.200800106 · Cited by 12
Gaikwad, V. V., & Bhanage, B. M. (2019) · Applied Organometallic Chemistry · doi:10.1002/aoc.4741 · Cited by 12
Zolfigol, M. A., Madrakian, E., Ghaemi, E., & Niknam, K. (2008) · Synthetic Communications · doi:10.1080/00397910802136706 · Cited by 11
Borges, E. L., Nobre, P. C., da Silva, M. S., Jacob, R. G., Lenardao, E. J., & Perin, G. (2016) · Journal of environmental chemical engineering · doi:10.1016/j.jece.2016.03.027 · Cited by 11
Li, K., Liu, C., Wang, K., Ren, Y., & Li, F. (2018) · RSC Advances · doi:10.1039/c8ra00905h · Cited by 11
Gupta, A., Bharadwaj, M., & Mehrotra, R. (2018) · Journal of Heterocyclic Chemistry · doi:10.1002/jhet.3424 · Cited by 11
Wei, T., Zhang, T., Huang, B., Tuo, Y., & Cai, M. (2015) · Applied Organometallic Chemistry · doi:10.1002/aoc.3394 · Cited by 10
Mallepalli, R., Vennam, D. K. R., & Perali, R. S. (2016) · Tetrahedron Letters · doi:10.1016/j.tetlet.2016.08.083 · Cited by 10
Ganapathi, M., Jayaseelan, D., & Guhanathan, S. (2015) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2015.05.002 · Cited by 9
Ponduri, R., Kumar, P., Vadali, L. R., & Modugu, N. R. (2018) · ChemistrySelect · doi:10.1002/slct.201801089 · Cited by 9
Ponduri, R., Kumar, P., & Vadali, L. R. (2018) · Synthetic Communications · doi:10.1080/00397911.2018.1535078 · Cited by 9
Li, K., Wang, K., Liu, C., Yang, X., Chen, X., Ren, Y., Cao, S., Liu, M., Tai, X., & Li, F. (2019) · Synthetic Communications · doi:10.1080/00397911.2018.1560875 · Cited by 8
Kumari, S., & Khurana, J. M. (2016) · Heteroatom Chemistry · doi:10.1002/hc.21351 · Cited by 7
Goodajdar, B. M., Akbari, F., & Davarpanah, J. (2018) · Applied Organometallic Chemistry · doi:10.1002/aoc.4647 · Cited by 7
Khan, T. A., & Siddiqui, Z. N. (2014) · Applied Organometallic Chemistry · doi:10.1002/aoc.3171 · Cited by 5
PEG-Solvent System for L-proline Catalyzed Wieland - Miescher Ketone Synthesis
Srivastava, V. (2014) · Current Organocatalysis · doi:10.2174/2213337201666140226000527 · Cited by 4
Revaprasadu, N., Chinnam, S., & Harika, P. (2015) · Asian Journal of Chemistry · doi:10.14233/ajchem.2016.19122 · Cited by 4
PEG-Supported Recyclable Catalyst for Enantioselective Ethylations
Zeng, X., Malik, D., Chen, R., & Lee‐Ruff, E. (2013) · Synthetic Communications · doi:10.1080/00397911.2011.625135 · Cited by 3
A Sustainable and Efficient Synthesis of Benzyl Phosphonates Using PEG/KI Catalytic System
Disale, S. T., Kale, S. R., Abraham, G., Kahandal, S. S., Sawarkar, A. N., & Gawande, M. B. (2016) · Frontiers in Chemistry · doi:10.3389/fchem.2016.00035 · Cited by 3
Coupled Unimolecular Dissociation Kinetics of Bromotoluene Radical Cations
Seo, J., Kim, S., & Shin, S. K. (2013) · The Journal of Physical Chemistry A · doi:10.1021/jp4031442 · Cited by 2
Research works printed but not linked: 9
- Lenick, 2019, vol. 14
- Kemisetti, 2018, J. Drug Deliv. Sci. Technol., 8, 145
- Z. Rapi, T.Nemcsok, P. Bagi, G. Keglevich, P. Bako 75 (2019), 3993–4004. · DOI
- Chikhale, 2013, S. Afr. J. Chem., 66, 254
- Goodajdar, 2018, Appl. Organomet. Chem., 32
- Bathula, 2015, Org. Chem., 11, 5
- Patil, 2019, Chemistry Select, 4, 11362
- Balaswamy, 2017, RASAYAN J. Chem., 10, 1134
- Nakkalwar, 2020, Asian J. Green Chem., 4, 159
Cited by
Sorted by citations
Modeling polyethylene glycol density using robust soft computing methods
Mohammad, A. A. S., Al-Daoud, K. I., Rusho, M. A., Alkhayyat, A., Doshi, H., Dey, P., Gagneja, K., Ramudu, M. J., Vasudevan, A., & Kiani, M. (2025) · Microchemical Journal · doi:10.1016/j.microc.2025.112815 · Cited by 130
Use of green alternative solvents in dispersive liquid‐liquid microextraction: A review
Grau, J., Azorín, C., Benedé, J. L., Chisvert, A., & Salvador, A. (2022) · Journal of Separation Science · doi:10.1002/jssc.202100609 · Cited by 131
Polyethylene glycol as a green chemical solvent
Hoffmann, M. M. (2021) · Current Opinion in Colloid & Interface Science · doi:10.1016/j.cocis.2021.101537 · Cited by 112
Rani, N., Duhan, A., Pal, A. K., Kumari, P., Kumar, R., Verma, D., Goyat, A., & Singh, R. (2023) · Journal of Cleaner Production · doi:10.1016/j.jclepro.2023.137232 · Cited by 87
Alqahtani, A. S. (2024) · Journal of Molecular Liquids · doi:10.1016/j.molliq.2024.124469 · Cited by 59
Metadata
- Authors
- Soni, J., Sahiba, N., Sethiya, A., & Agarwal, S.
- Affiliations
- Mohanlal Sukhadia University (IN)
- Corresponding author
- Agarwal, Shikha
- Venue
- Journal of Molecular Liquids
- Publisher
- Elsevier BV
- Published
- 2020-10
- Volume
- 315
- Pages
- 113766
- ISSN
- 0167-7322 (ISSN-L)
- OpenAlex
- W3041515436
- Cited by
- 107
- References
- 105
- Citations by year
- 2026: 13 · 2025: 22 · 2024: 33 · 2023: 20 · 2022: 11 · 2021: 7 · 2020: 1
- FWCI
- 3.79
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- Locations
- Journal of Molecular Liquids (publishedVersion)
- Funders
- Council of Scientific and Industrial Research, India (09/172(0088)/2018-EMR-I)
- University Grants Commission
- University Grants Committee (201819-MANF-2018-19-RAJ-91971)
- Topics
- Physical Sciences › Chemistry › Organic Chemistry › Chemical Synthesis and Reactions
- Physical Sciences › Chemistry › Organic Chemistry › Multicomponent Synthesis of Heterocycles
- Physical Sciences › Environmental Science › Environmental Chemistry › Chemistry and Chemical Engineering
- Keywords
- polyethylene glycol, green chemistry, heterogeneous catalysis, recyclable catalyst, biodegradable catalyst, green solvents, heterocyclic synthesis, sustainable organic synthesis
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