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For: Lipshutz BH. When Does Organic Chemistry Follow Nature’s Lead and “Make the Switch”? J Org Chem 2017;82:2806-16. [DOI: 10.1021/acs.joc.7b00010] [Cited by in Crossref: 61] [Cited by in F6Publishing: 31] [Article Influence: 12.2] [Reference Citation Analysis]
Number Citing Articles
1 Banerjee M, Panjikar PC, Bhutia ZT, Bhosle AA, Chatterjee A. Micellar nanoreactors for organic transformations with a focus on “dehydration” reactions in water: A decade update. Tetrahedron 2021;88:132142. [DOI: 10.1016/j.tet.2021.132142] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
2 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: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
3 Muzalevskiy VM, Belyaeva KV, Trofimov BA, Nenajdenko VG. Diastereoselective synthesis of CF 3 -oxazinoquinolines in water. Green Chem 2019;21:6353-60. [DOI: 10.1039/c9gc03044a] [Cited by in Crossref: 15] [Cited by in F6Publishing: 1] [Article Influence: 5.0] [Reference Citation Analysis]
4 Parmentier M, Gabriel CM, Guo P, Isley NA, Zhou J, Gallou F. Switching from organic solvents to water at an industrial scale. Current Opinion in Green and Sustainable Chemistry 2017;7:13-7. [DOI: 10.1016/j.cogsc.2017.06.004] [Cited by in Crossref: 16] [Cited by in F6Publishing: 10] [Article Influence: 3.2] [Reference Citation Analysis]
5 Akporji N, Thakore RR, Cortes-Clerget M, Andersen J, Landstrom E, Aue DH, Gallou F, Lipshutz BH. N2Phos - an easily made, highly effective ligand designed for ppm level Pd-catalyzed Suzuki-Miyaura cross couplings in water. Chem Sci 2020;11:5205-12. [PMID: 34122976 DOI: 10.1039/d0sc00968g] [Cited by in Crossref: 9] [Article Influence: 4.5] [Reference Citation Analysis]
6 Thakore RR, Takale BS, Gallou F, Reilly J, Lipshutz BH. N , C -Disubstituted Biarylpalladacycles as Precatalysts for ppm Pd-Catalyzed Cross Couplings in Water under Mild Conditions. ACS Catal 2019;9:11647-57. [DOI: 10.1021/acscatal.9b04204] [Cited by in Crossref: 25] [Cited by in F6Publishing: 16] [Article Influence: 8.3] [Reference Citation Analysis]
7 Wernik M, Sipos G, Buchholcz B, Darvas F, Novák Z, Ötvös SB, Kappe CO. Continuous flow heterogeneous catalytic reductive aminations under aqueous micellar conditions enabled by an oscillatory plug flow reactor. Green Chem 2021;23:5625-32. [DOI: 10.1039/d1gc02039k] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
8 Wood AB, Nandiwale KY, Mo Y, Jin B, Pomberger A, Schultz VL, Gallou F, Jensen KF, Lipshutz BH. Continuous flow Suzuki–Miyaura couplings in water under micellar conditions in a CSTR cascade catalyzed by Fe/ppm Pd nanoparticles. Green Chem 2020;22:3441-4. [DOI: 10.1039/d0gc00378f] [Cited by in Crossref: 12] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]
9 Ceriani C, Ghiglietti E, Sassi M, Mattiello S, Beverina L. Taming Troublesome Suzuki–Miyaura Reactions in Water Solution of Surfactants by the Use of Lecithin: A Step beyond the Micellar Model. Org Process Res Dev 2020;24:2604-10. [DOI: 10.1021/acs.oprd.0c00285] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 2.5] [Reference Citation Analysis]
10 Dissanayake DMMM, Melville AD, Vannucci AK. Electrochemical anion pool synthesis of amides with concurrent benzyl ester synthesis. Green Chem 2019;21:3165-71. [DOI: 10.1039/c9gc00707e] [Cited by in Crossref: 7] [Article Influence: 2.3] [Reference Citation Analysis]
11 Cortes-Clerget M, Akporji N, Zhou J, Gao F, Guo P, Parmentier M, Gallou F, Berthon JY, Lipshutz BH. Bridging the gap between transition metal- and bio-catalysis via aqueous micellar catalysis. Nat Commun 2019;10:2169. [PMID: 31092815 DOI: 10.1038/s41467-019-09751-4] [Cited by in Crossref: 50] [Cited by in F6Publishing: 31] [Article Influence: 16.7] [Reference Citation Analysis]
12 Gevorgyan A, Hopmann KH, Bayer A. Improved Buchwald–Hartwig Amination by the Use of Lipids and Lipid Impurities. Organometallics. [DOI: 10.1021/acs.organomet.1c00517] [Reference Citation Analysis]
13 Lipshutz BH, Ghorai S, Cortes-Clerget M. The Hydrophobic Effect Applied to Organic Synthesis: Recent Synthetic Chemistry "in Water". Chemistry 2018;24:6672-95. [PMID: 29465785 DOI: 10.1002/chem.201705499] [Cited by in Crossref: 136] [Cited by in F6Publishing: 61] [Article Influence: 34.0] [Reference Citation Analysis]
14 Asensio JM, Andrés R, Gómez-sal P, de Jesús E. Aqueous-Phase Chemistry of η 3 -Allylpalladium(II) Complexes with Sulfonated N -Heterocyclic Carbene Ligands: Solvent Effects in the Protolysis of Pd–C Bonds and Suzuki–Miyaura Reactions. Organometallics 2017;36:4191-201. [DOI: 10.1021/acs.organomet.7b00635] [Cited by in Crossref: 7] [Cited by in F6Publishing: 4] [Article Influence: 1.4] [Reference Citation Analysis]
15 Handa S, Jin B, Bora PP, Wang Y, Zhang X, Gallou F, Reilly J, Lipshutz BH. Sonogashira Couplings Catalyzed by Fe Nanoparticles Containing ppm Levels of Reusable Pd, under Mild Aqueous Micellar Conditions. ACS Catal 2019;9:2423-31. [DOI: 10.1021/acscatal.9b00007] [Cited by in Crossref: 47] [Cited by in F6Publishing: 32] [Article Influence: 15.7] [Reference Citation Analysis]
16 Thakore RR, Iyer KS, Lipshutz BH. Sustainable routes to amines in recyclable water using ppm Pd catalysis. Current Opinion in Green and Sustainable Chemistry 2021;31:100493. [DOI: 10.1016/j.cogsc.2021.100493] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
17 Yang Y, Meng X, Zhu B, Jia Y, Cao X, Huang S. A Micellar Catalysis Strategy for Amidation of Alkynyl Bromides: Synthesis of Ynamides in Water: A Micellar Catalysis Strategy for Amidation of Alkynyl Bromides: Synthesis of Ynamides in Water. Eur J Org Chem 2019;2019:1166-9. [DOI: 10.1002/ejoc.201801601] [Cited by in Crossref: 10] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
18 Lorenzetto T, Frigatti D, Fabris F, Scarso A. Nanoconfinement Effects of Micellar Media in Asymmetric Catalysis. Adv Synth Catal 2022;364:1776-97. [DOI: 10.1002/adsc.202200225] [Reference Citation Analysis]
19 Sherwood J, Clark JH, Fairlamb IJS, Slattery JM. Solvent effects in palladium catalysed cross-coupling reactions. Green Chem 2019;21:2164-213. [DOI: 10.1039/c9gc00617f] [Cited by in Crossref: 101] [Cited by in F6Publishing: 1] [Article Influence: 33.7] [Reference Citation Analysis]
20 Sheldon RA. The greening of solvents: Towards sustainable organic synthesis. Current Opinion in Green and Sustainable Chemistry 2019;18:13-9. [DOI: 10.1016/j.cogsc.2018.11.006] [Cited by in Crossref: 40] [Cited by in F6Publishing: 10] [Article Influence: 13.3] [Reference Citation Analysis]
21 Smith JD, Ansari TN, Andersson MP, Yadagiri D, Ibrahim F, Liang S, Hammond GB, Gallou F, Handa S. Micelle-enabled clean and selective sulfonylation of polyfluoroarenes in water under mild conditions. Green Chem 2018;20:1784-90. [DOI: 10.1039/c7gc03514d] [Cited by in Crossref: 38] [Article Influence: 9.5] [Reference Citation Analysis]
22 Sassi M, Mattiello S, Beverina L. Syntheses of Organic Semiconductors in Water. Recent Advancement in the Surfactants Enhanced Green Access to Polyconjugated Molecules: Syntheses of Organic Semiconductors in Water. Recent Advancement in the Surfactants Enhanced Green Access to Polyconjugated Molecules. Eur J Org Chem 2020;2020:3942-53. [DOI: 10.1002/ejoc.202000140] [Cited by in Crossref: 5] [Cited by in F6Publishing: 1] [Article Influence: 2.5] [Reference Citation Analysis]
23 Yu J, Iyer KS, Lipshutz BH. An environmentally responsible synthesis of the antitumor agent lapatinib (Tykerb). Green Chem . [DOI: 10.1039/d2gc00598k] [Reference Citation Analysis]
24 Lipshutz BH. Catalyst: Imagine Doing Chemistry at No Cost … to the Environment! Chem 2018;4:2004-7. [DOI: 10.1016/j.chempr.2018.08.031] [Cited by in Crossref: 19] [Cited by in F6Publishing: 9] [Article Influence: 4.8] [Reference Citation Analysis]
25 Rodygin KS, Ledovskaya MS, Voronin VV, Lotsman KA, Ananikov VP. Calcium Carbide: Versatile Synthetic Applications, Green Methodology and Sustainability. Eur J Org Chem 2021;2021:43-52. [DOI: 10.1002/ejoc.202001098] [Cited by in Crossref: 6] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
26 Borlinghaus N, Ansari TN, von Garrel LH, Ogulu D, Handa S, Wittmann V, Braje WM. Nucleophilic aromatic substitution reactions under aqueous, mild conditions using polymeric additive HPMC. Green Chem 2021;23:3955-62. [DOI: 10.1039/d1gc00128k] [Cited by in Crossref: 7] [Cited by in F6Publishing: 4] [Article Influence: 7.0] [Reference Citation Analysis]
27 Lipshutz BH. Illuminating a Path4914. Copyright 2016 Wiley for Organic Synthesis Towards Sustainability. No One Said It Would Be Easy…. Synlett 2021;32:1588-605. [DOI: 10.1055/s-0040-1706027] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
28 Bryan MC, Dunn PJ, Entwistle D, Gallou F, Koenig SG, Hayler JD, Hickey MR, Hughes S, Kopach ME, Moine G, Richardson P, Roschangar F, Steven A, Weiberth FJ. Key Green Chemistry research areas from a pharmaceutical manufacturers’ perspective revisited. Green Chem 2018;20:5082-103. [DOI: 10.1039/c8gc01276h] [Cited by in Crossref: 175] [Cited by in F6Publishing: 2] [Article Influence: 43.8] [Reference Citation Analysis]
29 Rooney M, Mattiello S, Stara R, Sanzone A, Brazzo P, Sassi M, Beverina L. Suzuki-Miyaura cross-coupling of latent pigments in water/toluene emulsion under aerobic atmosphere. Dyes and Pigments 2018;149:893-901. [DOI: 10.1016/j.dyepig.2017.11.044] [Cited by in Crossref: 14] [Cited by in F6Publishing: 6] [Article Influence: 3.5] [Reference Citation Analysis]
30 Belyaeva KV, Nikitina LP, Mal'kina AG, Afonin AV, Vashchenko AV, Trofimov BA. Cyanoacetylenes as Triggers and Partners in KOH-Assisted Assemblies of Quinoline-Based Dihydropyrimido[1,2-a]quinolin-3-ones on Water. J Org Chem 2019;84:9726-33. [PMID: 31262176 DOI: 10.1021/acs.joc.9b01482] [Cited by in Crossref: 8] [Article Influence: 2.7] [Reference Citation Analysis]
31 Borlinghaus N, Wittmann V, Braje WM. Using polymeric hydroxypropyl methylcellulose as an alternative to ‘micellar catalysis’ to enable chemical reactions in water. Current Opinion in Green and Sustainable Chemistry 2022;33:100571. [DOI: 10.1016/j.cogsc.2021.100571] [Reference Citation Analysis]
32 Lee NR, Moghadam FA, Braga FC, Lippincott DJ, Zhu B, Gallou F, Lipshutz BH. Sustainable Palladium-Catalyzed Tsuji-Trost Reactions Enabled by Aqueous Micellar Catalysis. Org Lett 2020;22:4949-54. [PMID: 32551706 DOI: 10.1021/acs.orglett.0c01329] [Cited by in Crossref: 9] [Cited by in F6Publishing: 2] [Article Influence: 4.5] [Reference Citation Analysis]
33 Alarcón‐matus E, Alvarado C, Romero‐ceronio N, Ramos‐rivera EM, Lobato‐garcía CE. Proline‐derived Long‐aliphatic‐chain Amphiphilic Organocatalysts (PDLACAOs) for Asymmetric Reactions in Aqueous Media. Asian J of Organic Chemis 2020;9:1667-87. [DOI: 10.1002/ajoc.202000419] [Cited by in Crossref: 4] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
34 Fantinel M, Valiati N, Moro PA, Sá MM. Amino-modified Merrifield resins as recyclable catalysts for the safe and sustainable preparation of functionalized α-diazo carbonyl compounds. Tetrahedron 2021;86:132081. [DOI: 10.1016/j.tet.2021.132081] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
35 Thakore RR, Takale BS, Hu Y, Ramer S, Kostal J, Gallou F, Lipshutz BH. “TPG-lite”: A new, simplified “designer” surfactant for general use in synthesis under micellar catalysis conditions in recyclable water. Tetrahedron 2021;87:132090. [DOI: 10.1016/j.tet.2021.132090] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
36 Andersson MP, Gallou F, Klumphu P, Takale BS, Lipshutz BH. Structure of Nanoparticles Derived from Designer Surfactant TPGS-750-M in Water, As Used in Organic Synthesis. Chemistry 2018;24:6778-86. [PMID: 29504665 DOI: 10.1002/chem.201705524] [Cited by in Crossref: 40] [Cited by in F6Publishing: 16] [Article Influence: 10.0] [Reference Citation Analysis]
37 Chen D, Zhang Y, Pan X, Wang F, Huang S. Oxidation of Tertiary Aromatic Alcohols to Ketones in Water. Adv Synth Catal 2018;360:3607-12. [DOI: 10.1002/adsc.201800612] [Cited by in Crossref: 14] [Cited by in F6Publishing: 10] [Article Influence: 3.5] [Reference Citation Analysis]
38 Pallini F, Sangalli E, Sassi M, Roth PMC, Mattiello S, Beverina L. Selective photoredox direct arylations of aryl bromides in water in a microfluidic reactor. Org Biomol Chem 2021;19:3016-23. [PMID: 33885555 DOI: 10.1039/d1ob00050k] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
39 Lippincott DJ, Landstrom E, Cortes-clerget M, Lipshutz BH, Buescher K, Schreiber R, Durano C, Parmentier M, Ye N, Wu B, Shi M, Yang H, Andersson M, Gallou F. Surfactant Technology: With New Rules, Designing New Sequences Is Required! Org Process Res Dev 2020;24:841-9. [DOI: 10.1021/acs.oprd.9b00454] [Cited by in Crossref: 15] [Article Influence: 5.0] [Reference Citation Analysis]
40 Wood AB, Roa DE, Gallou F, Lipshutz BH. α-Arylation of (hetero)aryl ketones in aqueous surfactant media. Green Chem 2021;23:4858-65. [DOI: 10.1039/d1gc01572a] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 6.0] [Reference Citation Analysis]
41 Manske C, Schmiedtchen M, Gellhaar S, Kiesel M, Becker J. Amide and Peptide Couplings Mediated by Pivaloyl Mixed Anhydrides in Aqueous Media. ACS Sustainable Chem Eng 2022;10:5307-14. [DOI: 10.1021/acssuschemeng.2c00642] [Reference Citation Analysis]
42 Takale BS, Thakore RR, Handa S, Gallou F, Reilly J, Lipshutz BH. A new, substituted palladacycle for ppm level Pd-catalyzed Suzuki-Miyaura cross couplings in water. Chem Sci 2019;10:8825-31. [PMID: 31803456 DOI: 10.1039/c9sc02528f] [Cited by in Crossref: 35] [Cited by in F6Publishing: 4] [Article Influence: 11.7] [Reference Citation Analysis]
43 Jimenez-gonzalez C. Life cycle considerations of solvents. Current Opinion in Green and Sustainable Chemistry 2019;18:66-71. [DOI: 10.1016/j.cogsc.2019.02.004] [Cited by in Crossref: 9] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
44 Cortes-Clerget M, Yu J, Kincaid JRA, Walde P, Gallou F, Lipshutz BH. Water as the reaction medium in organic chemistry: from our worst enemy to our best friend. Chem Sci 2021;12:4237-66. [PMID: 34163692 DOI: 10.1039/d0sc06000c] [Cited by in Crossref: 19] [Article Influence: 19.0] [Reference Citation Analysis]
45 Kincaid JRA, Kavthe RD, Caravez JC, Takale BS, Thakore RR, Lipshutz BH. Environmentally Responsible and Cost-Effective Synthesis of the Antimalarial Drug Pyronaridine. Org Lett 2022. [PMID: 35504038 DOI: 10.1021/acs.orglett.2c00944] [Reference Citation Analysis]
46 Lippincott DJ, Linstadt RTH, Maser MR, Gallou F, Lipshutz BH. Synthesis of Functionalized 1,3-Butadienes via Pd-Catalyzed Cross-Couplings of Substituted Allenic Esters in Water at Room Temperature. Org Lett 2018;20:4719-22. [PMID: 30080419 DOI: 10.1021/acs.orglett.8b01377] [Cited by in Crossref: 10] [Cited by in F6Publishing: 8] [Article Influence: 2.5] [Reference Citation Analysis]
47 Lee NR, Cortes-Clerget M, Wood AB, Lippincott DJ, Pang H, Moghadam FA, Gallou F, Lipshutz BH. Coolade. A Low-Foaming Surfactant for Organic Synthesis in Water. ChemSusChem 2019;12:3159-65. [PMID: 30889298 DOI: 10.1002/cssc.201900369] [Cited by in Crossref: 11] [Cited by in F6Publishing: 9] [Article Influence: 3.7] [Reference Citation Analysis]
48 Lorenzetto T, Frigatti D, Fabris F, Scarso A. Minimalistic β-Sitosterol based Designer Surfactants for Efficient Cross-Coupling in Water. Journal of Organometallic Chemistry 2022. [DOI: 10.1016/j.jorganchem.2022.122316] [Reference Citation Analysis]
49 Lipshutz BH. Synthetic chemistry in a water world. New rules ripe for discovery. Current Opinion in Green and Sustainable Chemistry 2018;11:1-8. [DOI: 10.1016/j.cogsc.2017.10.004] [Cited by in Crossref: 49] [Cited by in F6Publishing: 15] [Article Influence: 12.3] [Reference Citation Analysis]
50 Niu T, Chen S, Hong M, Zhang T, Chen J, Dong X, Ni B. Heterogeneous carbon nitride photocatalyst for C–C bond oxidative cleavage of vicinal diols in aerobic micellar medium. Green Chem 2020;22:5042-9. [DOI: 10.1039/d0gc01727b] [Cited by in Crossref: 12] [Article Influence: 6.0] [Reference Citation Analysis]
51 Wood AB, Plummer S, Robinson RI, Smith M, Chang J, Gallou F, Lipshutz BH. Continuous slurry plug flow Fe/ppm Pd nanoparticle-catalyzed Suzuki–Miyaura couplings in water utilizing novel solid handling equipment. Green Chem 2021;23:7724-30. [DOI: 10.1039/d1gc02461b] [Reference Citation Analysis]
52 Godha AK, Thiruvengadam J, Abhilash V, Balgi P, Narayanareddy AV, Vignesh K, Gadakh AV, Sathiyanarayanan AM, Ganesh S. Environmentally benign nucleophilic substitution reaction of arylalkyl halides in water using CTAB as the inverse phase transfer catalyst. New J Chem 2019;43:16041-5. [DOI: 10.1039/c9nj03941d] [Cited by in Crossref: 4] [Cited by in F6Publishing: 1] [Article Influence: 1.3] [Reference Citation Analysis]
53 Yang Z, Hu L, Cao T, An L, Li L, Yang T, Zhou C. PIDA-mediated α-C–H functionalization of enaminones: the synthesis of thiocyano enaminones and chromones in water. New J Chem 2019;43:16441-4. [DOI: 10.1039/c9nj04580e] [Cited by in Crossref: 12] [Cited by in F6Publishing: 2] [Article Influence: 4.0] [Reference Citation Analysis]
54 Hazra S, Gallou F, Handa S. Water: An Underestimated Solvent for Amide Bond-Forming Reactions. ACS Sustainable Chem Eng 2022;10:5299-306. [DOI: 10.1021/acssuschemeng.2c00520] [Reference Citation Analysis]
55 Calascibetta AM, Mattiello S, Sanzone A, Facchinetti I, Sassi M, Beverina L. Sustainable Access to π-Conjugated Molecular Materials via Direct (Hetero)Arylation Reactions in Water and under Air. Molecules 2020;25:E3717. [PMID: 32824058 DOI: 10.3390/molecules25163717] [Cited by in Crossref: 3] [Article Influence: 1.5] [Reference Citation Analysis]
56 Li Q, Zhang X, Xie K, Dai Q, Zeng R, Liu Y, Jia Z, Feng X, Li J. Diastereodivergent synthesis of cyclopropanes via on-water [2 + 1] annulations of diazo compounds with electron-deficient alkenes. Green Chem 2019;21:2375-9. [DOI: 10.1039/c9gc00278b] [Cited by in Crossref: 13] [Article Influence: 4.3] [Reference Citation Analysis]
57 Cortes-Clerget M, Lee NR, Lipshutz BH. Synthetic chemistry in water: applications to peptide synthesis and nitro-group reductions. Nat Protoc 2019;14:1108-29. [PMID: 30903108 DOI: 10.1038/s41596-019-0130-1] [Cited by in Crossref: 12] [Cited by in F6Publishing: 6] [Article Influence: 4.0] [Reference Citation Analysis]
58 Takale BS, Thakore RR, Gao ES, Gallou F, Lipshutz BH. Environmentally responsible, safe, and chemoselective catalytic hydrogenation of olefins: ppm level Pd catalysis in recyclable water at room temperature. Green Chem 2020;22:6055-61. [DOI: 10.1039/d0gc02087g] [Cited by in Crossref: 13] [Article Influence: 6.5] [Reference Citation Analysis]
59 Lee SY, Cheon C. On-Water Synthesis of 2-Substituted Quinolines from 2-Aminochalcones Using Benzylamine as the Nucleophilic Catalyst. J Org Chem 2018;83:13036-44. [DOI: 10.1021/acs.joc.8b01675] [Cited by in Crossref: 18] [Cited by in F6Publishing: 6] [Article Influence: 4.5] [Reference Citation Analysis]
60 Constable DJC. Green and sustainable chemistry - The case for a systems-based, interdisciplinary approach. iScience 2021;24:103489. [PMID: 34934914 DOI: 10.1016/j.isci.2021.103489] [Reference Citation Analysis]
61 Sanzone A, Calascibetta A, Ghiglietti E, Ceriani C, Mattioli G, Mattiello S, Sassi M, Beverina L. Suzuki–Miyaura Micellar One-Pot Synthesis of Symmetrical and Unsymmetrical 4,7-Diaryl-5,6-difluoro-2,1,3-benzothiadiazole Luminescent Derivatives in Water and under Air. J Org Chem 2018;83:15029-42. [DOI: 10.1021/acs.joc.8b02204] [Cited by in Crossref: 15] [Cited by in F6Publishing: 7] [Article Influence: 3.8] [Reference Citation Analysis]
62 Serrano-luginbühl S, Ruiz-mirazo K, Ostaszewski R, Gallou F, Walde P. Soft and dispersed interface-rich aqueous systems that promote and guide chemical reactions. Nat Rev Chem 2018;2:306-27. [DOI: 10.1038/s41570-018-0042-6] [Cited by in Crossref: 41] [Cited by in F6Publishing: 19] [Article Influence: 10.3] [Reference Citation Analysis]
63 Finck L, Brals J, Pavuluri B, Gallou F, Handa S. Micelle-Enabled Photoassisted Selective Oxyhalogenation of Alkynes in Water under Mild Conditions. J Org Chem 2018;83:7366-72. [DOI: 10.1021/acs.joc.7b03143] [Cited by in Crossref: 34] [Cited by in F6Publishing: 18] [Article Influence: 8.5] [Reference Citation Analysis]
64 Škopić MK, Götte K, Gramse C, Dieter M, Pospich S, Raunser S, Weberskirch R, Brunschweiger A. Micellar Brønsted Acid Mediated Synthesis of DNA-Tagged Heterocycles. J Am Chem Soc 2019;141:10546-55. [PMID: 31244181 DOI: 10.1021/jacs.9b05696] [Cited by in Crossref: 28] [Cited by in F6Publishing: 24] [Article Influence: 9.3] [Reference Citation Analysis]
65 Zuo W, Zhou J, Wu Y, Fang H, Lang X, Li Y, Zhan G, Han B. Synthesis of spiro(indoline-2,3′-hydropyridazine) via an “on-water” [4 + 2] annulation reaction. Org Chem Front 2021;8:922-7. [DOI: 10.1039/d0qo01422b] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]