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For: Nenajdenko VG, Muzalevskiy VM, Shastin AV. Polyfluorinated ethanes as versatile fluorinated C2-building blocks for organic synthesis. Chem Rev 2015;115:973-1050. [PMID: 25594605 DOI: 10.1021/cr500465n] [Cited by in Crossref: 102] [Cited by in F6Publishing: 66] [Article Influence: 14.6] [Reference Citation Analysis]
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7 Varun BV, Prabhu KR. Sulfur Assisted Tandem Electrophilic Fluorinative Deacylation: Synthesis of α-Fluoro β-Ketosulfides. J Org Chem 2017;82:9525-36. [DOI: 10.1021/acs.joc.7b01547] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 0.8] [Reference Citation Analysis]
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10 Lyakhovich MS, Murashkina AV, Panchenko SP, Averin AD, Abel AS, Maloshitskaya OA, Savelyev EN, Orlinson BS, Novakov IA, Beletskaya IP. Arylation of Adamantanamines: XI. Comparison of the Catalytic Efficiency of Palladium and Copper Complexes in Reactions of Adamantanamines with Fluorinated 2-Bromopyridines. Russ J Org Chem 2021;57:768-83. [DOI: 10.1134/s1070428021050031] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
11 Xu X, Liu F. Transition-metal-free radical tri-/difluoromethylation of N,N-dialkylhydrazones with sodium sulfinates. Org Chem Front 2017;4:2306-10. [DOI: 10.1039/c7qo00635g] [Cited by in Crossref: 23] [Article Influence: 4.6] [Reference Citation Analysis]
12 Pertusati F, Ferla S, Bassetto M, Brancale A, Khandil S, Westwell AD, Mcguigan C. A new series of bicalutamide, enzalutamide and enobosarm derivatives carrying pentafluorosulfanyl (SF5) and pentafluoroethyl (C2F5) substituents: Improved antiproliferative agents against prostate cancer. European Journal of Medicinal Chemistry 2019;180:1-14. [DOI: 10.1016/j.ejmech.2019.07.001] [Cited by in Crossref: 9] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
13 Wang Q, Ni C, Hu M, Xie Q, Liu Q, Pan S, Hu J. From C 1 to C 3 : Copper‐Catalyzed gem ‐Bis(trifluoromethyl)olefination of α‐Diazo Esters with TMSCF 3. Angew Chem 2020;132:8585-9. [DOI: 10.1002/ange.202002409] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 2.5] [Reference Citation Analysis]
14 Aldoshin AS, Tabolin AA, Ioffe SL, Nenajdenko VG. Green, Catalyst-Free Reaction of Indoles with β-Fluoro-β-nitrostyrenes in Water: Green, Catalyst-Free Reaction of Indoles with β-Fluoro-β-nitrostyrenes in Water. Eur J Org Chem 2018;2018:3816-25. [DOI: 10.1002/ejoc.201800385] [Cited by in Crossref: 13] [Cited by in F6Publishing: 7] [Article Influence: 3.3] [Reference Citation Analysis]
15 Arun V, Roy L, De Sarkar S. Alcohols as Fluoroalkyl Synthons: Ni-catalyzed Dehydrogenative Approach to Access Polyfluoroalkyl Bis-indoles. Chemistry 2020;26:16649-54. [PMID: 32914904 DOI: 10.1002/chem.202003912] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
16 Tong W, Huang Q, Li M, Wang J. Enzyme-catalyzed C–F bond formation and cleavage. Bioresour Bioprocess 2019;6. [DOI: 10.1186/s40643-019-0280-6] [Cited by in Crossref: 4] [Cited by in F6Publishing: 1] [Article Influence: 1.3] [Reference Citation Analysis]
17 Jiang D, Jia J, Wang B, Li B. Access to 5-fluoroalkylated trisubstituted oxazoles via copper-catalyzed cyclization of α-fluoroalkyl-α-diazoketones with amides. Chem Commun (Camb) 2022;58:4853-6. [PMID: 35348157 DOI: 10.1039/d2cc01057g] [Reference Citation Analysis]
18 Xiao Q, He Q, Li J, Wang J. 1,4-Diazabicyclo[2.2.2]octane-Promoted Aminotrifluoromethylthiolation of α,β-Unsaturated Carbonyl Compounds: N- Trifluoromethylthio-4-nitrophthalimide Acts as Both the Nitrogen and SCF 3 Sources. Org Lett 2015;17:6090-3. [DOI: 10.1021/acs.orglett.5b03116] [Cited by in Crossref: 44] [Cited by in F6Publishing: 29] [Article Influence: 6.3] [Reference Citation Analysis]
19 Antipin IS, Kazymova MA, Kuznetsov MA, Vasilyev AV, Ishchenko MA, Kiryushkin AA, Kuznetsova LM, Makarenko SV, Ostrovskii VA, Petrov ML, Solod OV, Trishin YG, Yakovlev IP, Nenaidenko VG, Beloglazkina EK, Beletskaya IP, Ustynyuk YA, Solov’ev PA, Ivanov IV, Malina EV, Sivova NV, Negrebetskii VV, Baukov YI, Pozharskaya NA, Traven’ VF, Shchekotikhin AE, Varlamov AV, Borisova TN, Lesina YA, Krasnokutskaya EA, Rogozhnikov SI, Shurov SN, Kustova TP, Klyuev MV, Khelevina OG, Stuzhin PA, Fedorov AY, Gushchin AV, Dodonov VA, Kolobov AV, Plakhtinskii VV, Orlov VY, Kriven’ko AP, Fedotova OV, Pchelintseva NV, Charushin VN, Chupakhin ON, Klimochkin YN, Klimochkina AY, Kuryatnikov VN, Malinovskaya YA, Levina AS, Zhuravlev OE, Voronchikhina LI, Fisyuk AS, Aksenov AV, Aksenov NA, Aksenova IV. Organic chemistry. History and mutual relations of universities of Russia. Russ J Org Chem 2017;53:1275-437. [DOI: 10.1134/s1070428017090019] [Cited by in Crossref: 39] [Article Influence: 9.8] [Reference Citation Analysis]
20 Yang J, Han QY, Zhao CL, Dong T, Hou ZY, Qin HL, Zhang CP. Pd-catalyzed divergent trifluoroethylation and arylation of arylboronic acids by aryl(2,2,2-trifluoroethyl)iodonium triflates. Org Biomol Chem 2016;14:7654-8. [PMID: 27384263 DOI: 10.1039/c6ob01384h] [Cited by in Crossref: 20] [Cited by in F6Publishing: 2] [Article Influence: 5.0] [Reference Citation Analysis]
21 Prieto A, Melot R, Bouyssi D, Monteiro N. C–H Difluoroalkylation of Aldehyde Hydrazones with Functionalized Difluoromethyl Bromides under Copper Catalysis. ACS Catal 2016;6:1093-6. [DOI: 10.1021/acscatal.5b02755] [Cited by in Crossref: 63] [Cited by in F6Publishing: 54] [Article Influence: 10.5] [Reference Citation Analysis]
22 Andriyankova LV, Nikitina LP, Belyaeva KV, Mal’kina AG, Afonin AV, Muzalevskii VM, Nenaidenko VG, Trofimov BA. Opening of the pyridine ring in the system 1,1,1-trifluoro-4-phenylbut-3-yn-2-one–water. Stereoselective synthesis of 5-{[(1Z)-4,4,4-trifluoro-3-oxo-1-phenylbut-1-en-1-yl]amino}penta-2,4-dienal. Russ J Org Chem 2016;52:1857-60. [DOI: 10.1134/s1070428016120289] [Cited by in Crossref: 7] [Cited by in F6Publishing: 1] [Article Influence: 1.4] [Reference Citation Analysis]
23 Kostromitin VS, Zemtsov AA, Kokorekin VA, Levin VV, Dilman AD. Atom-transfer radical addition of fluoroalkyl bromides to alkenes via a photoredox/copper catalytic system. Chem Commun (Camb) 2021;57:5219-22. [PMID: 33908970 DOI: 10.1039/d1cc01609a] [Cited by in Crossref: 3] [Article Influence: 3.0] [Reference Citation Analysis]
24 Maharramov AM, Shikhaliyev NQ, Suleymanova GT, Gurbanov AV, Babayeva GV, Mammadova GZ, Zubkov FI, Nenajdenko VG, Mahmudov KT, Pombeiro AJ. Pnicogen, halogen and hydrogen bonds in (E)-1-(2,2-dichloro-1-(2-nitrophenyl)vinyl)-2-(para-substituted phenyl)-diazenes. Dyes and Pigments 2018;159:135-41. [DOI: 10.1016/j.dyepig.2018.06.022] [Cited by in Crossref: 35] [Cited by in F6Publishing: 4] [Article Influence: 8.8] [Reference Citation Analysis]
25 Zhang Y, Ye X, Liu S, Chen W, Majeed I, Liu T, Zhu Y, Zeng Z. NaOTs-promoted transition metal-free C-N bond cleavage to form C-X (X = N, O, S) bonds. Org Biomol Chem 2021;19:8566-71. [PMID: 34550144 DOI: 10.1039/d1ob01409a] [Reference Citation Analysis]
26 Wang C, Zhang Y, Feng C. Fluorine Effects on Group Migration via a Rhodium(V) Nitrenoid Intermediate. Angew Chem 2017;129:15114-8. [DOI: 10.1002/ange.201708505] [Cited by in Crossref: 10] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
27 Glenadel Q, Billard T. Direct Perfluoroalkylthiolation of Few Chalcogenols. Chin J Chem 2016;34:455-8. [DOI: 10.1002/cjoc.201500913] [Cited by in Crossref: 10] [Cited by in F6Publishing: 6] [Article Influence: 1.7] [Reference Citation Analysis]
28 Zhou Y, Zhang C, Zhao Y, Li D, Zhao J, Wang Z, Qu J. Base-Promoted Double-Bond-Migration/Hydrolysis/Isomerization of 4-Aryl-1,1,1-trifluorobut-2-en-2-yl Trifluoromethanesulfonates: A Metal-Free Approach to β-Trifluoromethyl Ketones: Base-Promoted Double-Bond-Migration/Hydrolysis/Isomerization of 4-Aryl-1,1,1-trifluorobut-2-en-2-yl Trifluoromethanesulfonates: A Metal-Free Approach. Eur J Org Chem 2018;2018:6217-22. [DOI: 10.1002/ejoc.201801025] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
29 Meanwell NA. Fluorine and Fluorinated Motifs in the Design and Application of Bioisosteres for Drug Design. J Med Chem 2018;61:5822-80. [PMID: 29400967 DOI: 10.1021/acs.jmedchem.7b01788] [Cited by in Crossref: 630] [Cited by in F6Publishing: 432] [Article Influence: 157.5] [Reference Citation Analysis]
30 Mandal A, Selvakumar J, Dana S, Mukherjee U, Baidya M. A Cross-Dehydrogenative Annulation Strategy towards Synthesis of Polyfluorinated Phenanthridinones with Copper. Chemistry 2018;24:3448-54. [PMID: 29381235 DOI: 10.1002/chem.201800337] [Cited by in Crossref: 11] [Cited by in F6Publishing: 9] [Article Influence: 2.8] [Reference Citation Analysis]
31 Wang C, Zhang Y, Feng C. Fluorine Effects on Group Migration via a Rhodium(V) Nitrenoid Intermediate. Angew Chem Int Ed 2017;56:14918-22. [DOI: 10.1002/anie.201708505] [Cited by in Crossref: 38] [Cited by in F6Publishing: 23] [Article Influence: 7.6] [Reference Citation Analysis]
32 Aikawa K, Maruyama K, Nitta J, Hashimoto R, Mikami K. Siladifluoromethylation and Difluoromethylation onto C(sp(3)), C(sp(2)), and C(sp) Centers Using Ruppert-Prakash Reagent and Fluoroform. Org Lett 2016;18:3354-7. [PMID: 27340753 DOI: 10.1021/acs.orglett.6b01476] [Cited by in Crossref: 29] [Cited by in F6Publishing: 21] [Article Influence: 4.8] [Reference Citation Analysis]
33 Cui X, Shi J. Sn-based catalysts for Baeyer-Villiger oxidations by using hydrogen peroxide as oxidant. Sci China Mater 2016;59:675-700. [DOI: 10.1007/s40843-016-5081-x] [Cited by in Crossref: 8] [Cited by in F6Publishing: 6] [Article Influence: 1.3] [Reference Citation Analysis]
34 Li L, Huang M, Liu C, Xiao J, Chen Q, Guo Y, Zhao Z. 2,2,2-Trifluoroethylation of Styrenes with Concomitant Introduction of a Hydroxyl Group from Molecular Oxygen by Photoredox Catalysis Activated by Visible Light. Org Lett 2015;17:4714-7. [DOI: 10.1021/acs.orglett.5b02177] [Cited by in Crossref: 59] [Cited by in F6Publishing: 52] [Article Influence: 8.4] [Reference Citation Analysis]
35 Han E, Sun Y, Shen Q, Chen Q, Guo Y, Huang Y. Cu-Mediated 2,2,2-trifluoroethylation of terminal alkynes using 1,1-dichloro-2,2,2-trifluoroethane (HCFC-123). Org Chem Front 2015;2:1379-87. [DOI: 10.1039/c5qo00210a] [Cited by in Crossref: 18] [Article Influence: 2.6] [Reference Citation Analysis]
36 Wu X, Qiao K, Qin H, Zhang D, Gao D, Yang Z, Fang Z, Guo K. Silver( i )-mediated oxidative C(sp 3 )–H amination of ethers with azole derivatives under mild conditions. Org Chem Front 2019;6:2672-7. [DOI: 10.1039/c9qo00644c] [Cited by in Crossref: 4] [Article Influence: 1.3] [Reference Citation Analysis]
37 Qian J, Zhang J, Yang H, Kang L, Jiang G. Controlled chemoselective defluorination and non-defluorination for [5 + 1] aromatic annulation via Meisenheimer-type nitrogen anion and radical intermediates. Chem Sci 2019;10:8812-6. [PMID: 31803454 DOI: 10.1039/c9sc03216a] [Cited by in Crossref: 4] [Article Influence: 1.3] [Reference Citation Analysis]
38 Kutovaya IV, Shmatova OI, Tkachuk VM, Sukach VA, Vovk MV, Nenajdenko VG. Oxidative Nef reaction of trifluoromethylated 2-nitroalkanamines. Mendeleev Communications 2016;26:511-2. [DOI: 10.1016/j.mencom.2016.11.017] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
39 Muzalevskiy VM, Sizova ZA, Nenajdenko VG. An Efficient Synthesis of 2-CF3-3-Benzylindoles. Molecules 2021;26:5084. [PMID: 34443672 DOI: 10.3390/molecules26165084] [Reference Citation Analysis]
40 Chang B, Su Y, Huang D, Wang K, Zhang W, Shi Y, Zhang X, Hu Y. Synthesis of Trifluoroethyl Pyrazolines via Trichloroisocyanuric Acid Promoted Cascade Cyclization/Trifluoromethylation of β,γ-Unsaturated Hydrazones. J Org Chem 2018;83:4365-74. [DOI: 10.1021/acs.joc.8b00009] [Cited by in Crossref: 22] [Cited by in F6Publishing: 11] [Article Influence: 5.5] [Reference Citation Analysis]
41 Budinská A, Václavík J, Matoušek V, Beier P. Nucleophilic Tetrafluoroethylation Employing in Situ Formed Organomagnesium Reagents. Org Lett 2016;18:5844-7. [PMID: 27797526 DOI: 10.1021/acs.orglett.6b02890] [Cited by in Crossref: 24] [Cited by in F6Publishing: 16] [Article Influence: 4.0] [Reference Citation Analysis]
42 Luo Q, Liu C, Tong J, Shao Y, Shan W, Wang H, Zheng H, Cheng J, Wan X. Cu-Catalyzed Multicomponent Reaction of Styrenes, Perfluoroalkyl Halide, Alcohol, and tert -Butyl Hydroperoxide: One-Pot Synthesis of ( Z )-β-Alkoxyperfluoroalkenone. J Org Chem 2016;81:3103-11. [DOI: 10.1021/acs.joc.5b02664] [Cited by in Crossref: 15] [Cited by in F6Publishing: 13] [Article Influence: 2.5] [Reference Citation Analysis]
43 Sandzhieva MA, Kazakova AN, Boyarskaya IA, Ivanov AY, Nenajdenko VG, Vasilyev AV. Friedel-Crafts Alkylation of Arenes with 2-Halogeno-2-CF3-styrenes under Superacidic Conditions. Access to Trifluoromethylated Ethanes and Ethenes. J Org Chem 2016;81:5032-45. [PMID: 27227747 DOI: 10.1021/acs.joc.6b00419] [Cited by in Crossref: 15] [Article Influence: 2.5] [Reference Citation Analysis]
44 Varadwaj A, Varadwaj PR, Marques HM, Yamashita K. Revealing Factors Influencing the Fluorine-Centered Non-Covalent Interactions in Some Fluorine-Substituted Molecular Complexes: Insights from First-Principles Studies. Chemphyschem 2018;19:1486-99. [PMID: 29569853 DOI: 10.1002/cphc.201800023] [Cited by in Crossref: 10] [Cited by in F6Publishing: 6] [Article Influence: 2.5] [Reference Citation Analysis]
45 Liang H, Xu GQ, Feng ZT, Wang ZY, Xu PF. Dual Catalytic Switchable Divergent Synthesis: An Asymmetric Visible-Light Photocatalytic Approach to Fluorine-Containing γ-Keto Acid Frameworks. J Org Chem 2019;84:60-72. [PMID: 30507130 DOI: 10.1021/acs.joc.8b02316] [Cited by in Crossref: 21] [Cited by in F6Publishing: 12] [Article Influence: 5.3] [Reference Citation Analysis]
46 Rong J, Deng L, Tan P, Ni C, Gu Y, Hu J. Radical Fluoroalkylation of Isocyanides with Fluorinated Sulfones by Visible-Light Photoredox Catalysis. Angew Chem 2016;128:2793-7. [DOI: 10.1002/ange.201510533] [Cited by in Crossref: 58] [Cited by in F6Publishing: 43] [Article Influence: 9.7] [Reference Citation Analysis]
47 Rong J, Deng L, Tan P, Ni C, Gu Y, Hu J. Radical Fluoroalkylation of Isocyanides with Fluorinated Sulfones by Visible-Light Photoredox Catalysis. Angew Chem Int Ed 2016;55:2743-7. [DOI: 10.1002/anie.201510533] [Cited by in Crossref: 217] [Cited by in F6Publishing: 166] [Article Influence: 36.2] [Reference Citation Analysis]
48 Muzalevskiy VM, Belyaeva KV, Trofimov BA, Nenajdenko VG. Organometal-Free Arylation and Arylation/Trifluoroacetylation of Quinolines by Their Reaction with CF3-ynones and Base-Induced Rearrangement. J Org Chem 2020;85:9993-10006. [PMID: 32631065 DOI: 10.1021/acs.joc.0c01277] [Cited by in Crossref: 2] [Article Influence: 1.0] [Reference Citation Analysis]
49 Muzalevskiy VM, Shastin AV, Shikhaliev NG, Magerramov AM, Teymurova AN, Nenajdenko VG. Ionic liquids as a reusable media for copper catalysis. Green access to alkenes using catalytic olefination reaction. Tetrahedron 2016;72:7159-63. [DOI: 10.1016/j.tet.2016.09.050] [Cited by in Crossref: 8] [Cited by in F6Publishing: 2] [Article Influence: 1.3] [Reference Citation Analysis]
50 Muzalevskiy VM, Sizova ZA, Diusenov AI, Shastin AV, Nenajdenko VG. Efficient Multigram Approach to Acetylenes and CF 3 ‐ynones Starting from Dichloroalkenes Prepared by Catalytic Olefination Reaction (COR). Eur J Org Chem 2020;2020:4161-6. [DOI: 10.1002/ejoc.202000531] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
51 Gui J, Cai X, Chen L, Zhou Y, Zhu W, Jiang Y, Hu M, Chen X, Hu Y, Zhang S. Facile and practical hydrodehalogenations of organic halides enabled by calcium hydride and palladium chloride. Org Chem Front 2021;8:4685-92. [DOI: 10.1039/d1qo00758k] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
52 Zhang X, Wang X, Gao Y, Xu X. Silver-catalyzed formal [3+2]-cycloaddition of α-trifluoromethylated methyl isocyanides: a facile stereoselective synthesis of CF 3 -substituted heterocycles. Chem Commun 2017;53:2427-30. [DOI: 10.1039/c6cc10124k] [Cited by in Crossref: 36] [Article Influence: 7.2] [Reference Citation Analysis]
53 Yang J, Zhou X, Zeng Y, Huang C, Xiao Y, Zhang J. Divergent synthesis from reactions of 2-trifluoromethyl-1,3-conjugated enynes with N-acetylated 2-aminomalonates. Org Biomol Chem 2017;15:2253-8. [DOI: 10.1039/c6ob02749k] [Cited by in Crossref: 16] [Cited by in F6Publishing: 1] [Article Influence: 3.2] [Reference Citation Analysis]
54 Zhang JQ, Hu D, Song J, Ren H. [3 + 2]-Annulation of gem-Difluoroalkenes and Pyridinium Ylides: Access to Functionalized 2-Fluoroindolizines. J Org Chem 2021;86:4646-60. [PMID: 33683121 DOI: 10.1021/acs.joc.0c03041] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
55 Muzalevskiy VM, Sizova ZA, Panyushkin VV, Chertkov VA, Khrustalev VN, Nenajdenko VG. α,β-Disubstituted CF3-Enones as a Trifluoromethyl Building Block: Regioselective Preparation of Totally Substituted 3-CF3-Pyrazoles. J Org Chem 2021;86:2385-405. [PMID: 33423495 DOI: 10.1021/acs.joc.0c02516] [Cited by in Crossref: 4] [Article Influence: 4.0] [Reference Citation Analysis]
56 Muzalevskiy VM, Nenajdenko VG. Electrophilic halogenation of hydrazones of CF3-ynones. Regioselective synthesis of 4-halo-substituted 3-CF3-pyrazoles. Org Biomol Chem 2018;16:7935-46. [PMID: 30318541 DOI: 10.1039/c8ob02247j] [Cited by in Crossref: 11] [Cited by in F6Publishing: 1] [Article Influence: 2.8] [Reference Citation Analysis]
57 Haghighi F, Panahi F, Golbon Haghighi M, Khalafi-nezhad A. Transition metal-free N -fluoroalkylation of amines using cyanurate activated fluoroalcohols. Chem Commun 2017;53:12650-3. [DOI: 10.1039/c7cc07428j] [Cited by in Crossref: 10] [Article Influence: 2.0] [Reference Citation Analysis]
58 Zhang F, Lv N, Zheng Y, Ma J. Phosphine-Relayed Aldehyde-Olefination and Aza-Wittig Reaction with 2,2,2-Trifluorodiazoethane. Chin J Chem 2018;36:723-30. [DOI: 10.1002/cjoc.201800158] [Cited by in Crossref: 10] [Cited by in F6Publishing: 8] [Article Influence: 2.5] [Reference Citation Analysis]
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