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For: Mykhailiuk PK. Fluorinated Pyrazoles: From Synthesis to Applications. Chem Rev 2021;121:1670-715. [DOI: 10.1021/acs.chemrev.0c01015] [Cited by in Crossref: 84] [Cited by in F6Publishing: 88] [Article Influence: 42.0] [Reference Citation Analysis]
Number Citing Articles
1 Bykova LS, Kochnev IА, Barkov AY, Zimnitskiy NS, Korotaev VY, Sosnovskikh VY. An AgOAc-catalyzed reaction of 3-nitro-2H-chromenes with ethyl diazoacetate: an efficient one-pot synthesis of ethyl 3,4-dihydrochromeno[3,4-c]pyrazole-1-carboxylates. Chem Heterocycl Comp 2022. [DOI: 10.1007/s10593-022-03128-0] [Reference Citation Analysis]
2 Lam L, Park SH, Sloop J. Synthesis and Characterization of 3-Methyl-1-(4-(trifluoromethyl)phenyl)indeno [1,2-c]pyrazol-4(1H)-one. Molbank 2022;2022:M1483. [DOI: 10.3390/m1483] [Reference Citation Analysis]
3 Chen S, Li J, He Z, Chen G, Zhuang Y, Chen C, Liu Y. N-Trifluoropropylation of Azoles through N-Vinylation and Sequential Hydrogenation. J Org Chem 2022. [DOI: 10.1021/acs.joc.2c02323] [Reference Citation Analysis]
4 Ruffell K, Argent SP, Ling KB, Ball LT. Bismuth‐Mediated α‐Arylation of Acidic Diketones with ortho ‐Substituted Boronic Acids. Angew Chem Int Ed 2022;61. [DOI: 10.1002/anie.202210840] [Reference Citation Analysis]
5 Sun B, Zhuang X, Yin J, Zhang K, Zhao H, Jin C. Photoredox-Catalyzed Tandem Radical Cyclization/Hydroxylation for the Synthesis of 4-Hydroxyalkyl-3,3-difluoro-γ-lactams. J Org Chem 2022. [PMID: 36173277 DOI: 10.1021/acs.joc.2c01710] [Reference Citation Analysis]
6 Feng J, Wang Y, Gao L, Yu Y, Baell JB, Huang F. Electrochemical Synthesis of Polysubstituted Sulfonated Pyrazoles via Cascade Intermolecular Condensation, Radical-Radical Cross Coupling Sulfonylation, and Pyrazole Annulation. J Org Chem 2022. [PMID: 36166815 DOI: 10.1021/acs.joc.2c01609] [Reference Citation Analysis]
7 Ahmed AHH, Mohamed MFA, Allam RM, Nafady A, Mohamed SK, Gouda AE, Beshr EAM. Design, synthesis, and molecular docking of novel pyrazole-chalcone analogs of lonazolac as 5-LOX, iNOS and tubulin polymerization inhibitors with potential anticancer and anti-inflammatory activities. Bioorg Chem 2022;129:106171. [PMID: 36166898 DOI: 10.1016/j.bioorg.2022.106171] [Reference Citation Analysis]
8 Csenki JT, Tóth BL, Béke F, Varga B, P. Fehér P, Stirling A, Czégény Z, Bényei A, Novák Z. Synthesis of Hydrofluoroolefin‐Based Iodonium Reagent via Dyotropic Rearrangement and Its Utilization in Fluoroalkylation. Angew Chem Int Ed 2022;61. [DOI: 10.1002/anie.202208420] [Reference Citation Analysis]
9 Muravev AA, Ovsyannikov AS, Konorov GV, Islamov DR, Usachev KS, Novikov AS, Solovieva SE, Antipin IS. Thermodynamic vs. Kinetic Control in Synthesis of O-Donor 2,5-Substituted Furan and 3,5-Substituted Pyrazole from Heteropropargyl Precursor. Molecules 2022;27:5178. [PMID: 36014420 DOI: 10.3390/molecules27165178] [Reference Citation Analysis]
10 Wang X, Wang X, Pan H, Ming X, Zhang Z, Wang T. Palladium-Catalyzed Oxidative Nonclassical Heck Reaction of Arylhydrazines with Allylic Alcohols via C-N Bond Cleavage: Access to β-Arylated Carbonyl Compounds. J Org Chem 2022. [PMID: 35877650 DOI: 10.1021/acs.joc.2c01115] [Reference Citation Analysis]
11 Bychek R, Mykhailiuk PK. A Practical and Scalable Approach to Fluoro-Substituted Bicyclo[1.1.1]pentanes. Angew Chem Int Ed Engl 2022;61:e202205103. [PMID: 35638404 DOI: 10.1002/anie.202205103] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
12 Bazhin DN, Kudyakova YS, Edilova YO, Burgart YV, Saloutin VI. Fluorinated 1,2,4-triketone analogs: new prospects for heterocyclic and coordination chemistry. Russ Chem Bull 2022;71:1321-41. [DOI: 10.1007/s11172-022-3539-6] [Reference Citation Analysis]
13 Hong B, Ding X, Jiang M, Qin L, Lin Z, Wu W, Weng Z. A zinc-catalyzed synthesis of 3-trifluoromethyl-4-trifluoroacetyl pyrazoles. Tetrahedron Letters 2022. [DOI: 10.1016/j.tetlet.2022.154018] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
14 Xu Q, Zhang Z, Huang C, Bao Q, Zhang R, Wu M, Xiao X, Han X, Li X, Zhou J. Development of novel androgen receptor antagonists based on the structure of darolutamide. Bioorganic Chemistry 2022;124:105829. [DOI: 10.1016/j.bioorg.2022.105829] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
15 Mondal J, Sivaramakrishna A. Functionalized Triazines and Tetrazines: Synthesis and Applications. Top Curr Chem (Cham) 2022;380:34. [PMID: 35737142 DOI: 10.1007/s41061-022-00385-7] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
16 Bychek R, Mykhailiuk PK. A Practical and Scalable Approach to Fluoro‐Substituted Bicyclo[1.1.1]pentanes. Angewandte Chemie. [DOI: 10.1002/ange.202205103] [Reference Citation Analysis]
17 Meador RIL, Mate NA, Chisholm JD. Acid Catalyzed N-Alkylation of Pyrazoles with Trichloroacetimidates. Organics 2022;3:111-21. [DOI: 10.3390/org3020009] [Reference Citation Analysis]
18 Zheng Y, Long Y, Gong H, Xu J, Zhang C, Fu H, Zheng X, Chen H, Li R. Ruthenium-Catalyzed Divergent Acceptorless Dehydrogenative Coupling of 1,3-Diols with Arylhydrazines: Synthesis of Pyrazoles and 2-Pyrazolines. Org Lett 2022. [PMID: 35609118 DOI: 10.1021/acs.orglett.2c01497] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
19 Wang K, Liu H, Liu X, Bian C, Wang J, Su Y, Huang D, Hu Y. Regioselective Synthesis of 3‐Trifluoromethyl 4‐Subtituted Pyrazoles by [3+2] Cycloaddition of Trifluoroacetonitrile Imines and Nitroalkenes. Asian J of Organic Chemis 2022;11. [DOI: 10.1002/ajoc.202200103] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
20 Zhang D, Gao X, Min QQ, Gu Y, Berthon G, Zhang X. Coupling of Heteroaryl Halides with Chlorodifluoroacetamides and Chlorodifluoroacetate by Nickel Catalysis. Chemistry 2022;28:e202200642. [PMID: 35238111 DOI: 10.1002/chem.202200642] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
21 Mannava MKC, Bommaka MK, Dandela R, Solomon KA, Nangia AK. Fluorobenzoic acid coformers to improve the solubility and permeability of the BCS class IV drug naftopidil. Chem Commun (Camb) 2022;58:5582-5. [PMID: 35393986 DOI: 10.1039/d1cc07187d] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
22 Yang WF, Shu T, Chen HR, Qin HL, Tang H. A cascade reaction for regioselective construction of pyrazole-containing aliphatic sulfonyl fluorides. Org Biomol Chem 2022;20:3506-10. [PMID: 35420611 DOI: 10.1039/d2ob00515h] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
23 Kowalczyk A, Utecht-Jarzyńska G, Mlostoń G, Jasiński M. Trifluoromethylated Pyrazoles via Sequential (3 + 2)-Cycloaddition of Fluorinated Nitrile Imines with Chalcones and Solvent-Dependent Deacylative Oxidation Reactions. Org Lett 2022. [PMID: 35343703 DOI: 10.1021/acs.orglett.2c00521] [Cited by in Crossref: 4] [Cited by in F6Publishing: 7] [Article Influence: 4.0] [Reference Citation Analysis]
24 Borodkin GI, Shubin VG. Electrophilic Fluorination of Heterocyclic Compounds with NF Reagents in Unconventional Media. Chem Heterocycl Comp. [DOI: 10.1007/s10593-022-03060-3] [Reference Citation Analysis]
25 Mei H, Wang N, Li Z, Han J. Intramolecular Appel Reaction of Trifluoromethylated β-Keto Diazos Enabling Assembly of Trifluoromethylpyrazoles. Org Lett 2022. [PMID: 35297254 DOI: 10.1021/acs.orglett.2c00738] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
26 Mykhailiuk PK. Fluorine-Containing Prolines: Synthetic Strategies, Applications, and Opportunities. J Org Chem 2022. [PMID: 35175772 DOI: 10.1021/acs.joc.1c02956] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
27 Yamanushkin P, Kaya K, Feliciano MAM, Gold B. SuFExable NH-Pyrazoles via 1,3-Dipolar Cycloadditions of Diazo Compounds with Bromoethenylsulfonyl Fluoride. J Org Chem 2022. [PMID: 35143195 DOI: 10.1021/acs.joc.1c03105] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
28 Fang Z, Jin Q, Wang X, Ning Y. Metal-free [2 + 1 + 3] Cycloaddition of Trifluoroacetaldehyde N-Sulfonylhydrazones with Hexahydro-1,3,5-triazines Leading to Trifluoromethylated 2,3,4,5-Tetrahydro-1,2,4-triazines. J Org Chem 2022. [PMID: 35133818 DOI: 10.1021/acs.joc.1c02810] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
29 Yu D, Liu Y, Che C. Tungsten catalysed decarboxylative [3 + 2] cycloaddition aromatization: one-pot synthesis of trifluoromethyl-pyrrolo[2,1- a ]isoquinolines with visible light irradiation. Org Chem Front . [DOI: 10.1039/d2qo00401a] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
30 Itakhunov RN, Odin IS, Gusev DM, Grabovskiy SA, Gordon KV, Vologzhanina AV, Sokov SA, Sosnin IM, Golovanov AA. Cyclization of arylhydrazones of cross-conjugated enynones: synthesis of luminescent styryl-1H-pyrazoles and propenyl-1H-pyrazoles. Org Biomol Chem 2022. [DOI: 10.1039/d2ob01427k] [Reference Citation Analysis]
31 Wang C, Sun T, Zhang X, Yang X, Lu X, Xu H, Shi F, Zhang L, Ling Y. Design, Synthesis and Bioactivity of Novel Fluoropyrazole Hydrazides. Chinese Journal of Organic Chemistry 2022;42:1527. [DOI: 10.6023/cjoc202112021] [Reference Citation Analysis]
32 Edilova YO, Kudyakova YS, Kiskin MA, Burgart YV, Saloutin VI, Bazhin DN. Expanding 1,2,4-triketone toolbox for use as fluorinated building blocks in the synthesis of pyrazoles, pyridazinones and β-diketohydrazones. Journal of Fluorine Chemistry 2022;253:109932. [DOI: 10.1016/j.jfluchem.2021.109932] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
33 Gou Q, Zhu Q, Deng M, Li W, Ran X, Xie J, Huang H, Tan X, Zhu M. The regioselective annulation of N -methylpyridinium ylides with alkenes enabled by palladium catalysis: access to 3-unsubstituted indolizine derivatives. Org Chem Front . [DOI: 10.1039/d2qo00555g] [Reference Citation Analysis]
34 Chandrasekharan SP, Dhami A, Kumar S, Mohanan K. Recent advances in pyrazole synthesis employing diazo compounds and synthetic analogues. Org Biomol Chem 2022. [DOI: 10.1039/d2ob01918c] [Reference Citation Analysis]
35 Emashova SK, Titov AA, Smol'yakov AF, Chernyadyev AY, Godovikov IA, Godovikova MI, Dorovatovskii PV, Korlykov AA, Filippov OA, Shubina ES. Emissive silver( i ) cyclic trinuclear complexes with aromatic amine donor pyrazolate derivatives: way to efficiency. Inorg Chem Front . [DOI: 10.1039/d2qi01648f] [Reference Citation Analysis]
36 Zanatta N, Mittersteiner M, Aquino EC, Budragchaa T, Wessjohann LA, Bonacorso HG, Martins MAP. Synthesis of Methylene-Bridged Trifluoromethyl Azoles Using 5-(1,2,3-Triazol-1-yl)enones. Synthesis 2022;54:439-450. [DOI: 10.1055/s-0040-1719837] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
37 Gil-ordóñez M, Maestro A, Ortega P, Jambrina PG, Andrés JM. NHC-catalysed [3 + 2]-asymmetric annulation between pyrazolin-4,5-diones and enals: synthesis of novel spirocyclic pyrazolone γ-butyrolactones and computational study of mechanism and stereoselectivity. Org Chem Front 2022;9:420-7. [DOI: 10.1039/d1qo01462e] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
38 Tong C, Xu X, Qing F. Regioselective oxidative C–H heptafluoroisopropylation of heteroarenes with heptafluoroisopropyl silver. Org Chem Front . [DOI: 10.1039/d2qo00787h] [Reference Citation Analysis]
39 Akhmetova VR, Akhmadiev NS, Ibragimov AG. Sulfur-Containing Pyrazoles, Pyrazolines and Indazoles. N-Heterocycles 2022. [DOI: 10.1007/978-981-19-0832-3_7] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
40 Ryzhkova YE, Kalashnikova VM, Elinson MN. 6′-Amino-5,7-dibromo-2-oxo-3′-(trifluoromethyl)-1′H-spiro[indoline-3,4′-pyrano[2,3-c]pyrazole]-5′-carbonitrile. Molbank 2022;2022:M1309. [DOI: 10.3390/m1309] [Reference Citation Analysis]
41 Han T, Wang KH, Yang M, Zhao P, Wang F, Wang J, Huang D, Hu Y. Synthesis of Difluoromethylated Pyrazoles by the [3 + 2] Cycloaddition Reaction of Difluoroacetohydrazonoyl Bromides. J Org Chem 2021. [PMID: 34913680 DOI: 10.1021/acs.joc.1c02521] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 4.0] [Reference Citation Analysis]
42 O'Sullivan L, Patel KV, Rowley BC, Brownsey DK, Gorobets E, Gelfand BS, Van Humbeck JF, Derksen DJ. Regioselective Synthesis of C3-Hydroxyarylated Pyrazoles. J Org Chem 2021. [PMID: 34905376 DOI: 10.1021/acs.joc.1c02518] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
43 Shaitanova EN, Balabon OA, Rybakova AN, Khlebnicova TS, Lakhvich FA, Gerus II. Synthesis of functionalized fluoroalkyl pyrimidines and pyrazoles from fluoroalkyl enones. Journal of Fluorine Chemistry 2021;252:109905. [DOI: 10.1016/j.jfluchem.2021.109905] [Reference Citation Analysis]
44 Baranova KF, Titov AA, Smol'yakov AF, Chernyadyev AY, Filippov OA, Shubina ES. Mononuclear Copper(I) 3-(2-pyridyl)pyrazole Complexes: The Crucial Role of Phosphine on Photoluminescence. Molecules 2021;26:6869. [PMID: 34833961 DOI: 10.3390/molecules26226869] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
45 Zhang X, Sivaguru P, Zanoni G, Han X, Tong M, Bi X. Catalytic Asymmetric C(sp 3 )–H Carbene Insertion Approach to Access Enantioenriched 3-Fluoroalkyl 2,3-Dihydrobenzofurans. ACS Catal 2021;11:14293-301. [DOI: 10.1021/acscatal.1c04523] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 7.0] [Reference Citation Analysis]
46 Liu S, Tanabe Y, Kuriyama S, Sakata K, Nishibayashi Y. Ruthenium- and Copper-Catalyzed Propargylic Substitution Reactions of Propargylic Alcohol Derivatives with Hydrazones. Chemistry 2021;27:15650-9. [PMID: 34606139 DOI: 10.1002/chem.202103287] [Reference Citation Analysis]
47 Csenki JT, Mészáros Á, Gonda Z, Novák Z. Stereoselective Direct N-Trifluoropropenylation of Heterocycles with a Hypervalent Iodonium Reagent. Chemistry 2021;27:15638-43. [PMID: 34549840 DOI: 10.1002/chem.202102840] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
48 Noonikara-Poyil A, Muñoz-Castro A, Boretskyi A, Mykhailiuk PK, Dias HVR. When SF5 outplays CF3: effects of pentafluorosulfanyl decorated scorpionates on copper. Chem Sci 2021;12:14618-23. [PMID: 34881014 DOI: 10.1039/d1sc04846e] [Cited by in Crossref: 11] [Cited by in F6Publishing: 10] [Article Influence: 11.0] [Reference Citation Analysis]
49 Dasgupta A, Babaahmadi R, Pahar S, Stefkova K, Gierlichs L, Yates BF, Ariafard A, Melen RL. Tris(pentafluorphenyl)boran‐katalysierte Erzeugung von Carbenium‐Ionen und autokatalytische Pyrazol‐Synthese – eine theoretische und experimentelle Studie. Angew Chem 2021;133:24599-24604. [DOI: 10.1002/ange.202109744] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
50 Dasgupta A, Babaahmadi R, Pahar S, Stefkova K, Gierlichs L, Yates BF, Ariafard A, Melen RL. Tris(pentafluorophenyl)borane-Catalyzed Carbenium Ion Generation and Autocatalytic Pyrazole Synthesis-A Computational and Experimental Study. Angew Chem Int Ed Engl 2021;60:24395-9. [PMID: 34590773 DOI: 10.1002/anie.202109744] [Cited by in Crossref: 5] [Cited by in F6Publishing: 7] [Article Influence: 5.0] [Reference Citation Analysis]
51 Wang HZ, Li JZ, Guo Z, Zheng H, Wei WT. Visible-Light-Catalyzed N-Radical-Enabled Cyclization of Alkenes for the Synthesis of Five-Membered N-Heterocycles. ChemSusChem 2021;14:4658-70. [PMID: 34402206 DOI: 10.1002/cssc.202101586] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 8.0] [Reference Citation Analysis]
52 Yang K, Li Z, Sheng Y, Deng J, Song Y, Liu Z, Jia A. Construction of CF 3 ‐containing Oxepino[2,3‐ c ]pyrazole Motif via Sulfur Ylide‐mediated Annulation or Me 2 S involved One‐pot Reaction. Asian J of Organic Chemis 2021;10:3000-4. [DOI: 10.1002/ajoc.202100494] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
53 Shchegolkov EV, Burgart YV, Matsneva DA, Borisevich SS, Kadyrova RA, Orshanskaya IR, Zarubaev VV, Saloutin VI. Polyfluoroalkylated antipyrines in Pd-catalyzed transformations. RSC Adv 2021;11:35174-81. [PMID: 35493195 DOI: 10.1039/d1ra06967e] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
54 Borodkin GI, Shubin VG. Electrophilic and Oxidative Fluorination of Heterocyclic Compounds: Contribution to Green Chemistry. Russ J Org Chem 2021;57:1369-97. [DOI: 10.1134/s1070428021090013] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
55 Savych VI, Mykhalchuk VL, Melnychuk PV, Isakov AO, Savchuk T, Timoshenko VM, Siry SA, Pavlenko SO, Kovalenko DV, Hryshchuk OV, Reznik VA, Chalyk BA, Yarmolchuk VS, Rusanov EB, Mykhailiuk PK. Bicyclic Pyrrolidines for Medicinal Chemistry via [3 + 2]-Cycloaddition. J Org Chem 2021;86:13289-309. [PMID: 34428062 DOI: 10.1021/acs.joc.1c01327] [Cited by in Crossref: 6] [Cited by in F6Publishing: 3] [Article Influence: 6.0] [Reference Citation Analysis]
56 Borodkin Y, Institute of Organic Chemistry of the NAS of Ukraine, Rusanov E, Shermolovich Y. Isomeric bis(pyrazolyl)sulfones based on bis(1,1-dihydropolyfluoroalkyl)sulfones. A new type of ligands for metal-polymer complexes with silver cation. Vopr Khim Khim Tekhnol 2021. [DOI: 10.32434/0321-4095-2021-138-5-21-29] [Reference Citation Analysis]
57 Chen SJ, Golden DL, Krska SW, Stahl SS. Copper-Catalyzed Cross-Coupling of Benzylic C-H Bonds and Azoles with Controlled N-Site Selectivity. J Am Chem Soc 2021;143:14438-44. [PMID: 34464528 DOI: 10.1021/jacs.1c07117] [Cited by in Crossref: 14] [Cited by in F6Publishing: 14] [Article Influence: 14.0] [Reference Citation Analysis]
58 Trofymchuk S, Bugera M, Klipkov AA, Ahunovych V, Razhyk B, Semenov S, Boretskyi A, Tarasenko K, Mykhailiuk PK. Scalable Approach to Fluorinated Heterocycles with Sulfur Tetrafluoride (SF4). J Org Chem 2021;86:12181-98. [PMID: 34424702 DOI: 10.1021/acs.joc.1c01518] [Cited by in Crossref: 7] [Cited by in F6Publishing: 3] [Article Influence: 7.0] [Reference Citation Analysis]
59 Zheng C, Jiang C, Huang S, Zhao K, Fu Y, Ma M, Hong J. Transition-Metal-Free Synthesis of Aryl Trifluoromethyl Thioethers through Indirect Trifluoromethylthiolation of Sodium Arylsulfinate with TMSCF3. Org Lett 2021;23:6982-6. [PMID: 34474573 DOI: 10.1021/acs.orglett.1c02656] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
60 Sivaguru P, Bi X. Fluoroalkyl N-sulfonyl hydrazones: An efficient reagent for the synthesis of fluoroalkylated compounds. Sci China Chem 2021;64:1614-29. [DOI: 10.1007/s11426-021-1052-7] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 7.0] [Reference Citation Analysis]
61 Wang X, Zhou M, Liu Q, Ni C, Fei Z, Li W, Hu J. Deoxyfluorination of alcohols with aryl fluorosulfonates. Chem Commun (Camb) 2021;57:8170-3. [PMID: 34318800 DOI: 10.1039/d1cc02617h] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
62 Li Y, Zhang CL, Huang WH, Sun N, Hao M, Neumann H, Beller M. A general strategy for the synthesis of α-trifluoromethyl- and α-perfluoroalkyl-β-lactams via palladium-catalyzed carbonylation. Chem Sci 2021;12:10467-73. [PMID: 34447539 DOI: 10.1039/d1sc02212a] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]
63 Mittersteiner M, Bonacorso HG, Martins MAP, Zanatta N. Haloacetylated Enol Ethers: a Way Out for the Regioselective Synthesis of Biologically Active Heterocycles. Eur J Org Chem 2021;2021:3886-911. [DOI: 10.1002/ejoc.202100495] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 5.0] [Reference Citation Analysis]
64 Chen YJ, Zhang FG, Ma JA. Zinc-Enabled Annulation of Trifluorodiazoethane with 2H-Azirines to Construct Trifluoromethyl Pyrazolines, Pyrazoles, and Pyridazines. Org Lett 2021;23:6062-6. [PMID: 34319752 DOI: 10.1021/acs.orglett.1c02139] [Cited by in Crossref: 11] [Cited by in F6Publishing: 7] [Article Influence: 11.0] [Reference Citation Analysis]
65 Zhang X, Wang H, Xie L, You C, Han X, Weng Z. Copper-Catalyzed Synthesis of 5-Aryl-6-(Trifluoromethyl)-2,3-Dihydropyrazolo[1,2-a]Pyrazol-1(5H)-One. Chem Asian J 2021. [PMID: 34313007 DOI: 10.1002/asia.202100693] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
66 Guo H, Zhang Q, Pan W, Yang H, Pei K, Zhai J, Li T, Wang Z, Wang Y, Yin Y. One‐pot Synthesis of Substituted Pyrazoles from Propargyl Alcohols via Cyclocondensation of in situ‐Generated α‐Iodo Enones/Enals and Hydrazine Hydrate. Asian J Org Chem 2021;10:2231-7. [DOI: 10.1002/ajoc.202100318] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
67 Agafonova NA, Burgart YV, Gerasimova NA, Evstigneeva NP, Saloutin VI. Alternative approaches to the synthesis of polyfluoroalkyl-containing 1-methyl-4-nitrosopyrazoles. Russ Chem Bull 2021;70:1135-40. [DOI: 10.1007/s11172-021-3195-2] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
68 Gulia N, Małecki M, Szafert S. Direct Preparation of N-Substituted Pyrazoles from Primary Aliphatic or Aromatic Amines. J Org Chem 2021;86:9353-9. [PMID: 34197110 DOI: 10.1021/acs.joc.1c00606] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
69 Chen J, Chen D, Kuang J, Ma Y. Transition Metal-Free De Novo Synthesis of Sulfonated Pyrazoles from Sulfonyl Hydrazides, 1,3-Diketones, and Sodium Sulfinates at Room Temperature. J Org Chem 2021;86:9289-98. [PMID: 34185538 DOI: 10.1021/acs.joc.1c00171] [Cited by in Crossref: 6] [Cited by in F6Publishing: 2] [Article Influence: 6.0] [Reference Citation Analysis]
70 Zhang X, Tian C, Wang Z, Sivaguru P, Nolan SP, Bi X. Fluoroalkyl N -Triftosylhydrazones as Easily Decomposable Diazo Surrogates for Asymmetric [2 + 1] Cycloaddition: Synthesis of Chiral Fluoroalkyl Cyclopropenes and Cyclopropanes. ACS Catal 2021;11:8527-37. [DOI: 10.1021/acscatal.1c01483] [Cited by in Crossref: 12] [Cited by in F6Publishing: 13] [Article Influence: 12.0] [Reference Citation Analysis]
71 Utecht-Jarzyńska G, Nagła K, Mlostoń G, Heimgartner H, Palusiak M, Jasiński M. A straightforward conversion of 1,4-quinones into polycyclic pyrazoles via [3 + 2]-cycloaddition with fluorinated nitrile imines. Beilstein J Org Chem 2021;17:1509-17. [PMID: 34285722 DOI: 10.3762/bjoc.17.108] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
72 Plaçais C, Donnard M, Panossian A, Vors JP, Bernier D, Pazenok S, Leroux FR. Synthesis of 3-Amino-5-fluoroalkylfurans by Intramolecular Cyclization. Org Lett 2021;23:4915-9. [PMID: 34080423 DOI: 10.1021/acs.orglett.1c01672] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
73 Cao T, Yang Z, Sun Y, Zhao N, Lu S, Zhang J, Wang L. Lewis Base‐Catalyzed Cycloaddition of Heterocyclic Alkenes with 2,2,2‐Trifluorodiazoethane (CF 3 CHN 2 ): Access to Trifluoromethylated Pyrazolines and Pyrazoles. Eur J Org Chem 2021;2021:2950-4. [DOI: 10.1002/ejoc.202100521] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
74 Chinnam AK, Staples RJ, Shreeve JM. Selective Synthesis of Bis(3-(3-(trifluoromethyl)-1H-1,2,4-triazol-5-yl)-4,4'-azo- and -azoxyfurazan Derivatives. J Org Chem 2021;86:7781-6. [PMID: 34009988 DOI: 10.1021/acs.joc.1c00531] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 7.0] [Reference Citation Analysis]
75 Ren S, Xu G, Guo Y, Liu Q, Guo C. Iron porphyrin-catalyzed N-trifluoroethylation of anilines with 2,2,2-trifluoroethylamine hydrochloride in aqueous solution. RSC Adv 2021;11:20322-5. [PMID: 35479926 DOI: 10.1039/d1ra03379d] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
76 Alexander JR, Kevorkian PV, Topczewski JJ. Intercepting the Banert cascade with nucleophilic fluorine: direct access to α-fluorinated NH-1,2,3-triazoles. Chem Commun (Camb) 2021;57:5024-7. [PMID: 33890592 DOI: 10.1039/d1cc01179k] [Reference Citation Analysis]
77 Zheng Y, Xie Z, He X, Chen Y, Cheng W, Chen K, Xiang H, Chen X, Yang H. Phosphonium Ylide-Mediated Programmable Fluorination to Access Mono- and Difluoromethylarenes. Org Lett 2021;23:2538-42. [DOI: 10.1021/acs.orglett.1c00457] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
78 Wan C, Pang JY, Jiang W, Zhang XW, Hu XG. Copper-Catalyzed Reductive Ring-Cleavage of Isoxazoles: Synthesis of Fluoroalkylated Enaminones and Application for the Preparation of Celecoxib, Deracoxib, and Mavacoxib. J Org Chem 2021;86:4557-66. [PMID: 33586981 DOI: 10.1021/acs.joc.0c02980] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 8.0] [Reference Citation Analysis]
79 Tian Y, Li J, Zhang F, Ma J. Regioselective Decarboxylative Cycloaddition Route to Fully Substituted 3‐CF 3 ‐Pyrazoles from Nitrilimines and Isoxazolidinediones. Adv Synth Catal 2021;363:2093-7. [DOI: 10.1002/adsc.202100091] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 6.0] [Reference Citation Analysis]
80 Niu K, Ding L, Zhou P, Hao Y, Liu Y, Song H, Wang Q. Electro-oxidative C–H azolation of quinoxalin-2(1 H )-ones. Green Chem 2021;23:3246-9. [DOI: 10.1039/d1gc00861g] [Cited by in Crossref: 22] [Cited by in F6Publishing: 25] [Article Influence: 22.0] [Reference Citation Analysis]
81 Das S. Beyond conventional construction of the phthalimide core: a review. New J Chem 2021;45:20519-36. [DOI: 10.1039/d1nj03924e] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]