BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Jordan A, Stoy P, Sneddon HF. Chlorinated Solvents: Their Advantages, Disadvantages, and Alternatives in Organic and Medicinal Chemistry. Chem Rev 2021;121:1582-622. [DOI: 10.1021/acs.chemrev.0c00709] [Cited by in Crossref: 28] [Cited by in F6Publishing: 20] [Article Influence: 14.0] [Reference Citation Analysis]
Number Citing Articles
1 Brumovský M, Micić V, Oborná J, Filip J, Hofmann T, Tunega D. Iron nitride nanoparticles for rapid dechlorination of mixed chlorinated ethene contamination. Journal of Hazardous Materials 2023;442:129988. [DOI: 10.1016/j.jhazmat.2022.129988] [Reference Citation Analysis]
2 Mostafa A, Shaaban H, Alqarni AM, Alghamdi M, Alsultan S, Saleh Al-saeed J, Alsaba S, Almoslem A, Alshehry Y, Ahmad R. Vortex-assisted dispersive liquid–liquid microextraction using thymol based natural deep eutectic solvent for trace analysis of sulfonamides in water samples: Assessment of the greenness profile using AGREE metric, GAPI and analytical eco-scale. Microchemical Journal 2022;183:107976. [DOI: 10.1016/j.microc.2022.107976] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
3 Yin X, Hua H, Dyer J, Landis R, Fennell D, Axe L. Degradation of Chlorinated Solvents with Reactive Iron Minerals in Subsurface Sediments from Redox Transition Zones. Journal of Hazardous Materials 2022. [DOI: 10.1016/j.jhazmat.2022.130470] [Reference Citation Analysis]
4 Nguyen T, Sreekumar S, Wang S, Jiang Q, Montel F, Buono F. Enantioselective Synthesis of trans -Disubstituted Cyclopropyltrifluoroborate Building Blocks through Ru-Catalyzed Cyclopropanation. Org Process Res Dev . [DOI: 10.1021/acs.oprd.2c00265] [Reference Citation Analysis]
5 Dalla Torre D, Annatelli M, Aricò F. Acid catalyzed synthesis of dimethyl isosorbide via dimethyl carbonate chemistry. Catalysis Today 2022. [DOI: 10.1016/j.cattod.2022.08.034] [Reference Citation Analysis]
6 Almeida LD, Delolo FG, Costa AP, Gusevskaya EV, Robles-azocar PA. Catalytic aerobic epoxidation of bio-renewable alkenes using organic carbonates as green solvents. Molecular Catalysis 2022;527:112400. [DOI: 10.1016/j.mcat.2022.112400] [Reference Citation Analysis]
7 Jensen DL, Trinderup HH, Skovbo F, Jensen HH. Solvent free, catalytic and diastereoselective preparation of aryl and alkyl thioglycosides as key components for oligosaccharide synthesis. Org Biomol Chem 2022;20:4915-25. [PMID: 35678647 DOI: 10.1039/d2ob00939k] [Reference Citation Analysis]
8 Kerkel F, Kunz W, Kanzler W. Grüne Chemie: Mit Gamma‐Valerolacton lösen. Nachr Chem 2022;70:32-34. [DOI: 10.1002/nadc.20224119228] [Reference Citation Analysis]
9 Lou F, Cao Q, Zhang C, Ai N, Wang Q, Zhang J. Continuous synthesis of benzaldehyde by ozonolysis of styrene in a micro-packed bed reactor. J Flow Chem. [DOI: 10.1007/s41981-022-00220-6] [Reference Citation Analysis]
10 Timofeeva M, Gorbunova I, Alekseevskiy P, Shipilovskikh DA, Shipilovskikh SA. Large scale application of triphenylphosphine oxide thin films for a modified catalytic Appel reaction. Photonics and Nanostructures - Fundamentals and Applications 2022. [DOI: 10.1016/j.photonics.2022.101026] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
11 Verma A, Dolui P, Hazra S, Elias AJ. Directing group enabled ‘On-Water’ C-H bond functionalization of ferrocene derivatives. Journal of Organometallic Chemistry 2022. [DOI: 10.1016/j.jorganchem.2022.122303] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
12 Jordan A, Hall CGJ, Thorp LR, Sneddon HF. Replacement of Less-Preferred Dipolar Aprotic and Ethereal Solvents in Synthetic Organic Chemistry with More Sustainable Alternatives. Chem Rev 2022. [PMID: 35201751 DOI: 10.1021/acs.chemrev.1c00672] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 7.0] [Reference Citation Analysis]
13 Lane MKM, Garedew M, Deary EC, Coleman CN, Ahrens-Víquez MM, Erythropel HC, Zimmerman JB, Anastas PT. What to Expect When Expecting in Lab: A Review of Unique Risks and Resources for Pregnant Researchers in the Chemical Laboratory. Chem Res Toxicol 2022. [PMID: 35130693 DOI: 10.1021/acs.chemrestox.1c00380] [Reference Citation Analysis]
14 Becker J, Manske C, Randl S. Green chemistry and sustainability metrics in the pharmaceutical manufacturing sector. Current Opinion in Green and Sustainable Chemistry 2022;33:100562. [DOI: 10.1016/j.cogsc.2021.100562] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 9.0] [Reference Citation Analysis]
15 Velez C, Acevedo O. Simulation of deep eutectic solvents: Progress to promises. WIREs Comput Mol Sci. [DOI: 10.1002/wcms.1598] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
16 Ciriani M, Oliveira R, Afonso CAM. Semi-continuous and continuous processes for enantiomeric separation. Green Chem 2022;24:4328-62. [DOI: 10.1039/d1gc03668h] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
17 Sheldon RA. Biocatalysis, solvents, and green metrics in sustainable chemistry. Biocatalysis in Green Solvents 2022. [DOI: 10.1016/b978-0-323-91306-5.00012-1] [Reference Citation Analysis]
18 Winterton N. The green solvent: a critical perspective. Clean Technol Environ Policy 2021;:1-24. [PMID: 34608382 DOI: 10.1007/s10098-021-02188-8] [Cited by in Crossref: 13] [Cited by in F6Publishing: 14] [Article Influence: 13.0] [Reference Citation Analysis]
19 Tseke K, Lennon C, O'mahony J, Kinsella M. A Continuous‐Flow Route to Enantioenriched 3‐Substituted‐3‐Hydroxyoxindoles: Organocatalytic Aldol Reactions of Isatin with Acetone. Eur J Org Chem 2021;2021:5767-74. [DOI: 10.1002/ejoc.202100735] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
20 Crowley DC, Brouder TA, Kearney AM, Lynch D, Ford A, Collins SG, Maguire AR. Exploiting Continuous Processing for Challenging Diazo Transfer and Telescoped Copper-Catalyzed Asymmetric Transformations. J Org Chem 2021. [PMID: 34379975 DOI: 10.1021/acs.joc.1c01310] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
21 Zhang Y, Ozcer P, Ghoshal S. A comprehensive assessment of the degradation of C1 and C2 chlorinated hydrocarbons by sulfidated nanoscale zerovalent iron. Water Res 2021;201:117328. [PMID: 34171646 DOI: 10.1016/j.watres.2021.117328] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 5.0] [Reference Citation Analysis]
22 Gevorgyan A, Hopmann KH, Bayer A. Lipids as versatile solvents for chemical synthesis. Green Chem 2021;23:7219-27. [DOI: 10.1039/d1gc02311j] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 4.0] [Reference Citation Analysis]
23 Annatelli M, Dalla Torre D, Musolino M, Aricò F. Dimethyl isosorbide via organocatalyst N -methyl pyrrolidine: scaling up, purification and concurrent reaction pathways. Catal Sci Technol 2021;11:3411-21. [DOI: 10.1039/d1cy00465d] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 10.0] [Reference Citation Analysis]
24 Polterauer D, Roberge DM, Hanselmann P, Elsner P, Hone CA, Kappe CO. Process intensification of ozonolysis reactions using dedicated microstructured reactors. React Chem Eng 2021;6:2253-8. [DOI: 10.1039/d1re00264c] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
25 Manujyothi R, Aneeja T, Anilkumar G. Solvent-free synthesis of propargylamines: an overview. RSC Adv 2021;11:19433-49. [DOI: 10.1039/d1ra03324g] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 8.0] [Reference Citation Analysis]
26 Jordan A, Whymark KD, Sydenham J, Sneddon HF. A solvent-reagent selection guide for Steglich-type esterification of carboxylic acids. Green Chem 2021;23:6405-13. [DOI: 10.1039/d1gc02251b] [Cited by in Crossref: 5] [Cited by in F6Publishing: 8] [Article Influence: 5.0] [Reference Citation Analysis]
27 Gao F, Ferlin F, Bai R, Li M, Vaccaro L, Gu Y. Replacing halogenated solvents by a butyl acetate solution of bisphenol S in the transformations of indoles. Green Chem 2021;23:3588-94. [DOI: 10.1039/d1gc00778e] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 4.0] [Reference Citation Analysis]
28 Pourhossein M, Heravizadeh OR, Omidi F, Khadem M, Shahtaheri SJ. Ultrasound-Assisted Emulsified Microextraction Based on Deep Eutectic Solvent for Trace Residue Analysis of Metribuzin in Urine Samples. MOCA 2021;16:153-61. [DOI: 10.17721/moca.2021.153-161] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]