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For: Motornov VA, Tabolin AA, Novikov RA, Nelyubina YV, Ioffe SL, Smolyar IV, Nenajdenko VG. Synthesis and Regioselective N-2 Functionalization of 4-Fluoro-5-aryl-1,2,3-N H -triazoles: Synthesis and Regioselective N-2 Functionalization of 4-Fluoro-5-aryl-1,2,3-N H -triazoles. Eur J Org Chem 2017;2017:6851-60. [DOI: 10.1002/ejoc.201701338] [Cited by in Crossref: 22] [Cited by in F6Publishing: 9] [Article Influence: 4.4] [Reference Citation Analysis]
Number Citing Articles
1 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]
2 Kuritsyna MA, Pelipko VV, Kataeva ON, Baichurin RI, Sadikov KD, Smirnov AS, Makarenko SV. Ethyl 3-halo-3-nitroacrylates: synthesis and reactions with primary aromatic amines. Russ Chem Bull 2021;70:1605-12. [DOI: 10.1007/s11172-021-3257-5] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
3 Motornov VA, Tabolin AA, Nelyubina YV, Nenajdenko VG, Ioffe SL. Acid‐Mediated Three Component Assembly of 4‐Fluoropyrazoles from α‐Fluoronitroalkenes, Hydrazines, and Aldehydes. Eur J Org Chem 2020;2020:5211-9. [DOI: 10.1002/ejoc.202000841] [Cited by in Crossref: 5] [Article Influence: 2.5] [Reference Citation Analysis]
4 Jana S, Adhikari S, Cox MR, Roy S. Regioselective synthesis of 4-fluoro-1,5-disubstituted-1,2,3-triazoles from synthetic surrogates of α-fluoroalkynes. Chem Commun 2020;56:1871-4. [DOI: 10.1039/c9cc09216a] [Cited by in Crossref: 8] [Article Influence: 4.0] [Reference Citation Analysis]
5 Motornov V, Latyshev GV, Kotovshchikov YN, Lukashev NV, Beletskaya IP. Copper(I)‐Catalyzed Regioselective Chan‐Lam N 2‐Vinylation of 1,2,3‐Triazoles and Tetrazoles. Adv Synth Catal 2019;361:3306-11. [DOI: 10.1002/adsc.201900225] [Cited by in Crossref: 10] [Cited by in F6Publishing: 4] [Article Influence: 3.3] [Reference Citation Analysis]
6 Souza ROMA, Miranda LSME. Strategies Towards the Synthesis of N2-Substituted 1,2,3-Triazoles. An Acad Bras Cienc 2019;91:e20180751. [PMID: 30785471 DOI: 10.1590/0001-3765201820180751] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 1.7] [Reference Citation Analysis]
7 Avula SK, Khan A, Halim SA, Al-abri Z, Anwar MU, Al-rawahi A, Csuk R, Al-harrasi A. Synthesis of novel (R)-4-fluorophenyl-1H-1,2,3-triazoles: A new class of α-glucosidase inhibitors. Bioorganic Chemistry 2019;91:103182. [DOI: 10.1016/j.bioorg.2019.103182] [Cited by in Crossref: 12] [Cited by in F6Publishing: 7] [Article Influence: 4.0] [Reference Citation Analysis]
8 Reddy RJ, Shankar A, Waheed M, Nanubolu JB. Metal-free, highly regioselective sulfonylation of NH-1,2,3-triazoles with sodium sulfinates and thiosulfonates. Tetrahedron Letters 2018;59:2014-7. [DOI: 10.1016/j.tetlet.2018.04.023] [Cited by in Crossref: 19] [Article Influence: 4.8] [Reference Citation Analysis]
9 Motornov VA, Tabolin AA, Nelyubina YV, Nenajdenko VG, Ioffe SL. Copper-mediated oxidative [3 + 2]-annulation of nitroalkenes and pyridinium ylides: general access to functionalized indolizines and efficient synthesis of 1-fluoroindolizines. Org Biomol Chem 2019;17:1442-54. [PMID: 30672946 DOI: 10.1039/c8ob03126f] [Cited by in Crossref: 20] [Cited by in F6Publishing: 4] [Article Influence: 6.7] [Reference Citation Analysis]
10 Motornov VA, Tabolin AA, Novikov RA, Shepel NE, Nenajdenko VG, Ioffe SL. Synthesis of 2,5-diaryl-4-halo-1,2,3-triazoles and comparative study of their fluorescent properties. Tetrahedron 2018;74:3897-903. [DOI: 10.1016/j.tet.2018.05.071] [Cited by in Crossref: 6] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
11 Zheng Y, Tian L, Ramadoss V, Zhang H, Zhu L, Wang Y. Recent Developments in N2-Selective Functionalizations of 1,2,3-Triazoles. Synthesis 2022;54:2548-60. [DOI: 10.1055/s-0040-1719902] [Reference Citation Analysis]
12 Fujita T, Takeishi M, Ichikawa J. Copper-Catalyzed [3 + 2] Annulation of Azides with a (Difluorovinyl)zinc Complex, Fluoroacetylene Equivalent. Org Lett 2020;22:9253-7. [PMID: 33226831 DOI: 10.1021/acs.orglett.0c03476] [Cited by in Crossref: 3] [Article Influence: 1.5] [Reference Citation Analysis]
13 Roshandel S, Lunn MJ, Rasul G, Muthiah Ravinson DS, Suri SC, Prakash GKS. Catalyst-Free Regioselective N2 Arylation of 1,2,3-Triazoles Using Diaryl Iodonium Salts. Org Lett 2019;21:6255-8. [PMID: 31386386 DOI: 10.1021/acs.orglett.9b02140] [Cited by in Crossref: 13] [Cited by in F6Publishing: 7] [Article Influence: 4.3] [Reference Citation Analysis]
14 Zhang C, Zheng L, Yan Q, Hu Q, Jia F, Chen Y. A Direct P 2 O 5 -Mediated Synthesis of Diverse Sulfur-Containing Triazoles via Alkylation of NH -1,2,3-triazoles with Dimethyl Sulfoxide. ChemistrySelect 2018;3:10277-80. [DOI: 10.1002/slct.201802875] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 0.8] [Reference Citation Analysis]
15 Motornov VA, Tabolin AA, Nelyubina YV, Nenajdenko VG, Ioffe SL. Copper-mediated oxidative [3 + 2]-annulation of nitroalkenes and pyridinium imines: efficient synthesis of 3-fluoro- and 3-nitro-pyrazolo[1,5-a]pyridines. Org Biomol Chem 2020;18:1436-48. [PMID: 32022079 DOI: 10.1039/c9ob02668a] [Cited by in Crossref: 9] [Cited by in F6Publishing: 2] [Article Influence: 4.5] [Reference Citation Analysis]
16 Rai V, P K, Harmalkar SS, Dhuri SN, Maddani MR. 1,6-Addition of 1,2,3-NH triazoles to para-quinone methides: Facile access to highly selective N1 and N2 substituted triazoles. Org Biomol Chem 2022;20:345-51. [PMID: 34908078 DOI: 10.1039/d1ob01717a] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
17 Motornov VA, Tabolin AA, Nelyubina YV, Nenajdenko VG, Ioffe SL. Copper-catalyzed [3 + 2]-cycloaddition of α-halonitroalkenes with azomethine ylides: facile synthesis of multisubstituted pyrrolidines and pyrroles. Org Biomol Chem 2021;19:3413-27. [PMID: 33899878 DOI: 10.1039/d1ob00146a] [Cited by in Crossref: 3] [Article Influence: 3.0] [Reference Citation Analysis]