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For: Belskaya N, Subbotina J, Lesogorova S. Synthesis of 2H-1,2,3-Triazoles. In: Dehaen W, Bakulev VA, editors. Chemistry of 1,2,3-triazoles. Cham: Springer International Publishing; 2015. pp. 51-116. [DOI: 10.1007/7081_2014_125] [Cited by in Crossref: 29] [Cited by in F6Publishing: 12] [Article Influence: 3.6] [Reference Citation Analysis]
Number Citing Articles
1 Safronov NE, Fomin TO, Minin AS, Todorov L, Kostova I, Benassi E, Belskaya NP. 5-Amino-2-aryl-1,2,3-triazol-4-carboxylic acids: Synthesis, photophysical properties, and application prospects. Dyes and Pigments 2020;178:108343. [DOI: 10.1016/j.dyepig.2020.108343] [Cited by in Crossref: 5] [Cited by in F6Publishing: 1] [Article Influence: 2.5] [Reference Citation Analysis]
2 Gup R, Erer O, Dilek N. A rapid synthesis of 2-substituted 1,2,3- triazole-1-oxide derivative starting from 4-(methyl)isonitrosoacetophenone and its Ni(II) complex: Characterization, DNA binding and cleavage properties. Journal of Molecular Structure 2017;1129:142-51. [DOI: 10.1016/j.molstruc.2016.09.066] [Cited by in Crossref: 15] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
3 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]
4 Shafran YM, Silaichev PS, Bakulev VA. β-(Cycloalkylamino)ethanesulfonyl azides as novel water-soluble reagents for the synthesis of diazo compounds and heterocycles. Chem Heterocycl Comp 2019;55:1251-61. [DOI: 10.1007/s10593-019-02609-z] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.7] [Reference Citation Analysis]
5 Ilkin VG, Dianova LN, Bakulev VA, Berseneva VS, Saveliev DA, Beryozkina TV. The Dimroth rearrangement of 5-amino-1-aryl-1,2,3-triazole-4-carbothioamides. Chem Heterocycl Comp 2020;56:1335-40. [DOI: 10.1007/s10593-020-02819-w] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
6 Kuruba BK, Emmanuvel L, Sridhar B, Vasanthkumar S. Unprecedented cyclization of α -diazo hydrazones upon N-H functionalization: A Et 3 N base promoted one-step synthetic approach for the synthesis of N-amino-1,2,3-triazole derivatives from α -diazo hydrazone. Tetrahedron 2017;73:2674-81. [DOI: 10.1016/j.tet.2017.03.061] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 0.8] [Reference Citation Analysis]
7 Lopes AB, Wagner P, Kümmerle AE, Bihel F, Bourguignon J, Schmitt M, Miranda LSM. Development of a L-Tryptophan-Based Ligand for Regioselective Copper Catalyzed N 2 -Arylation of 1,2,3-Triazoles. ChemistrySelect 2017;2:6544-8. [DOI: 10.1002/slct.201701498] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 0.8] [Reference Citation Analysis]
8 Gavlik KD, Lesogorova SG, Sukhorukova ES, Subbotina JO, Slepukhin PA, Benassi E, Belskaya NP. Synthesis of 2-Aryl-1,2,3-triazoles by Oxidative Cyclization of 2-(Arylazo)ethene-1,1-diamines: A One-Pot Approach. Eur J Org Chem 2016;2016:2700-10. [DOI: 10.1002/ejoc.201600256] [Cited by in Crossref: 13] [Cited by in F6Publishing: 5] [Article Influence: 2.2] [Reference Citation Analysis]
9 Kang T, Kim H, Lee D. Triazoliptycenes: A Twist on Iptycene Chemistry for Regioselective Cross-Coupling To Build Nonstacking Fluorophores. Org Lett 2017;19:6380-3. [PMID: 29144765 DOI: 10.1021/acs.orglett.7b03239] [Cited by in Crossref: 8] [Cited by in F6Publishing: 3] [Article Influence: 1.6] [Reference Citation Analysis]
10 Hemmaragala NM, Abrahamse H, George BPA, Gannimani R, Govender P. Functionalized Silver Nanoparticle Catalyzed [3+2] Cycloaddition Reaction: Greener Route to Substituted-1,2,3-triazolines. Catal Lett 2016;146:464-73. [DOI: 10.1007/s10562-015-1653-x] [Cited by in Crossref: 3] [Article Influence: 0.4] [Reference Citation Analysis]
11 Silaichev PS, Beryozkina TV, Novikov MS, Dehaen W, Bakulev VA. A Base‐Controlled Reaction of 2‐Cyanoacetamidines (3,3‐Diaminoacrylonitriles) with Sulfonyl Azides as a Route to Nonaromatic 4‐Methylene‐1,2,3‐triazole‐5‐imines. Eur J Org Chem 2020;2020:3688-98. [DOI: 10.1002/ejoc.202000453] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
12 Stasevych MV, Zvarych VI, Lunin VV, Khomyak SV, Vovk MV, Novikov VP. Synthesis of pyrazole and tetrazole derivatives of 9,10-anthraquinonylhydrazones. Chem Heterocycl Comp 2017;53:927-9. [DOI: 10.1007/s10593-017-2148-z] [Cited by in Crossref: 7] [Cited by in F6Publishing: 1] [Article Influence: 1.4] [Reference Citation Analysis]
13 Bakulev VA, Beryozkina TA. NH-1,2,3-triazoles: synthesis and reactions with electrophilic agents. Chem Heterocycl Comp 2016;52:4-6. [DOI: 10.1007/s10593-016-1821-y] [Cited by in Crossref: 15] [Cited by in F6Publishing: 4] [Article Influence: 2.5] [Reference Citation Analysis]
14 Eltyshev AK, Suntsova PO, Karmatskaia KD, Taniya OS, Slepukhin PA, Benassi E, Belskaya NP. An effective and facile synthesis of new blue fluorophores on the basis of an 8-azapurine core. Org Biomol Chem 2018;16:9420-9. [PMID: 30500034 DOI: 10.1039/c8ob02644k] [Cited by in Crossref: 7] [Article Influence: 1.8] [Reference Citation Analysis]
15 Bennett JM, Shapiro JD, Choinski KN, Mei Y, Aulita SM, Reinheimer EW, Majireck MM. Synthesis of phthalan and phenethylamine derivatives via addition of alcohols to rhodium(II)-azavinyl carbenoids. Tetrahedron Letters 2017;58:1117-22. [DOI: 10.1016/j.tetlet.2017.01.105] [Cited by in Crossref: 9] [Cited by in F6Publishing: 4] [Article Influence: 1.8] [Reference Citation Analysis]
16 Sambiagio C, Schönbauer D, Blieck R, Dao-Huy T, Pototschnig G, Schaaf P, Wiesinger T, Zia MF, Wencel-Delord J, Besset T, Maes BUW, Schnürch M. A comprehensive overview of directing groups applied in metal-catalysed C-H functionalisation chemistry. Chem Soc Rev 2018;47:6603-743. [PMID: 30033454 DOI: 10.1039/c8cs00201k] [Cited by in Crossref: 703] [Cited by in F6Publishing: 66] [Article Influence: 175.8] [Reference Citation Analysis]
17 Francis DV, Harper JB, Read RW. Titration characteristics of fluorous 1,2,3-triazol-4-ylmethyl ethers, bis(1,2,3-triazol-4-ylmethyl) ethers and bis(1,2,3-triazol-4-ylmethyl) amines. Journal of Fluorine Chemistry 2016;192:86-97. [DOI: 10.1016/j.jfluchem.2016.10.012] [Reference Citation Analysis]
18 Thomas J, Jana S, Liekens S, Dehaen W. A single-step acid catalyzed reaction for rapid assembly of NH-1,2,3-triazoles. Chem Commun 2016;52:9236-9. [DOI: 10.1039/c6cc03744e] [Cited by in Crossref: 50] [Cited by in F6Publishing: 5] [Article Influence: 8.3] [Reference Citation Analysis]
19 Gavlik KD, Sukhorukova ES, Shafran YM, Slepukhin PA, Benassi E, Belskaya NP. 2-Aryl-5-amino-1,2,3-triazoles: New effective blue-emitting fluorophores. Dyes and Pigments 2017;136:229-42. [DOI: 10.1016/j.dyepig.2016.08.015] [Cited by in Crossref: 21] [Article Influence: 4.2] [Reference Citation Analysis]
20 Eltyshev AK, Minin AS, Smoliuk LT, Benassi E, Belskaya NP. 2-Aryl-2,4-dihydro-5 H -[1,2,3]triazolo[4,5- d ]pyrimidin-5-ones as a New Platform for the Design and Synthesis of Biosensors and Chemosensors: 2-Aryl-2,4-dihydro-5 H -[1,2,3]triazolo[4,5- d ]pyrimidin-5-ones as a New Platform for the Design and Synthesis of Biosensors and Chemosensors. Eur J Org Chem 2020;2020:316-29. [DOI: 10.1002/ejoc.201901582] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
21 Nagarajan R, Jayashankaran J, Emmanuvel L. Transition metal-free steric controlled one-pot synthesis of highly substituted N -amino 1,2,3-triazole derivatives via diazo transfer reaction from β-keto esters. Tetrahedron Letters 2016;57:2612-5. [DOI: 10.1016/j.tetlet.2016.04.112] [Cited by in Crossref: 10] [Cited by in F6Publishing: 3] [Article Influence: 1.7] [Reference Citation Analysis]
22 Filimonov VO, Dianova LN, Beryozkina TV, Mazur D, Beliaev NA, Volkova NN, Ilkin VG, Dehaen W, Lebedev AT, Bakulev VA. Water/Alkali-Catalyzed Reactions of Azides with 2-Cyanothioacetamides. Eco-Friendly Synthesis of Monocyclic and Bicyclic 1,2,3-Thiadiazole-4-carbimidamides and 5-Amino-1,2,3-triazole-4-carbothioamides. J Org Chem 2019;84:13430-46. [PMID: 31547663 DOI: 10.1021/acs.joc.9b01599] [Cited by in Crossref: 6] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]