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For: Srivastava A, Aggarwal L, Jain N. One-Pot Sequential Alkynylation and Cycloaddition: Regioselective Construction and Biological Evaluation of Novel Benzoxazole–Triazole Derivatives. ACS Comb Sci 2015;17:39-48. [DOI: 10.1021/co500135z] [Cited by in Crossref: 27] [Cited by in F6Publishing: 16] [Article Influence: 3.4] [Reference Citation Analysis]
Number Citing Articles
1 Wang A, Zhu Y, Wang S, Hao W, Li G, Tu S, Jiang B. Metal-Free Radical Haloazidation of Benzene-Tethered 1,7-Enynes Leading to Polyfunctionalized 3,4-Dihydroquinolin-2(1 H )-ones. J Org Chem 2016;81:1099-105. [DOI: 10.1021/acs.joc.5b02655] [Cited by in Crossref: 61] [Cited by in F6Publishing: 40] [Article Influence: 10.2] [Reference Citation Analysis]
2 Esmaeelzadeh M, Salehi P, Bararjanian M, Gharaghani S. Synthesis of new triazole tethered derivatives of curcumin and their antibacterial and antifungal properties. J IRAN CHEM SOC 2019;16:465-77. [DOI: 10.1007/s13738-018-1524-7] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 0.8] [Reference Citation Analysis]
3 Prabhakaran P, Subaraja M, Rajakumar P. Synthesis, Electrochemical, Antibacterial and Anticancer Studies on Triazole-Bridged Pyrrolidine-Grafted Macrocycles via [3+2] Cycloaddition of Azomethin Ylide. ChemistrySelect 2018;3:4687-93. [DOI: 10.1002/slct.201800033] [Cited by in Crossref: 6] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
4 Zaki M, Allouchi H, El Bouakher A, Duverger E, El Hakmaoui A, Daniellou R, Guillaumet G, Akssira M. Synthesis and anticancer evaluation of novel 9α-substituted-13-(1,2,3-triazolo)-parthenolides. Tetrahedron Letters 2016;57:2591-4. [DOI: 10.1016/j.tetlet.2016.04.115] [Cited by in Crossref: 7] [Cited by in F6Publishing: 2] [Article Influence: 1.2] [Reference Citation Analysis]
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6 Morri AK, Thummala Y, Doddi VR. The Dual Role of 1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU) in the Synthesis of Terminal Aryl- and Styryl-Acetylenes via Umpolung Reactivity. Org Lett 2015;17:4640-3. [DOI: 10.1021/acs.orglett.5b02398] [Cited by in Crossref: 46] [Cited by in F6Publishing: 22] [Article Influence: 6.6] [Reference Citation Analysis]
7 Talha A, Mourhly A, Tachallait H, Driowya M, El Hamidi A, Arshad S, Karrouchi K, Arsalane S, Bougrin K. One-pot four-component tandem synthesis of novel sulfonamide-1, 2, 3-triazoles catalyzed by reusable copper (II)-adsorbed on mesoporous silica under ultrasound irradiation. Tetrahedron 2021;90:132215. [DOI: 10.1016/j.tet.2021.132215] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
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9 Reddy RJ, Kumari AH, Kumar JJ, Nanubolu JB. Cs 2 CO 3 ‐Mediated Vicinal Thiosulfonylation of 1,1‐Dibromo‐1‐Alkenes with Thiosulfonates: An Expedient Synthesis of ( E )‐1,2‐Thiosulfonylethenes. Adv Synth Catal 2019;361:1587-91. [DOI: 10.1002/adsc.201801620] [Cited by in Crossref: 21] [Cited by in F6Publishing: 15] [Article Influence: 7.0] [Reference Citation Analysis]
10 Wei W, Li Q, Zhang M, He W. N-Radical enabled cyclization of 1,n-enynes. Chinese Journal of Catalysis 2021;42:731-42. [DOI: 10.1016/s1872-2067(20)63702-0] [Cited by in Crossref: 11] [Article Influence: 11.0] [Reference Citation Analysis]
11 Aziz J, Baladi T, Piguel S. Direct Alkynylation of 3 H -Imidazo[4,5- b ]pyridines Using gem -Dibromoalkenes as Alkynes Source. J Org Chem 2016;81:4122-33. [DOI: 10.1021/acs.joc.6b00406] [Cited by in Crossref: 16] [Cited by in F6Publishing: 9] [Article Influence: 2.7] [Reference Citation Analysis]
12 Singh M, Hazra A, Bharitkar YP, Kalia R, Sahoo A, Saha S, Ravichandiran V, Ghosh S, Mondal NB. Synthesis of diversely substituted bis-pyrrolizidino/ thiopyrrolizidino oxindolo/acenaphthyleno curcuminoids via sequential azomethine ylide cycloaddition. RSC Adv 2018;8:18938-51. [DOI: 10.1039/c8ra02725k] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
13 Jardosh HH, Vala ND, Patel MP. Library design, synthesis and biological exploration of novel 3,4′-bicarbostyril derivatives as potent antimicrobial, antitubercular and antimalarial agents. Med Chem Res 2017;26:881-99. [DOI: 10.1007/s00044-017-1797-x] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.4] [Reference Citation Analysis]
14 Dheer D, Singh V, Shankar R. Medicinal attributes of 1,2,3-triazoles: Current developments. Bioorg Chem 2017;71:30-54. [PMID: 28126288 DOI: 10.1016/j.bioorg.2017.01.010] [Cited by in Crossref: 360] [Cited by in F6Publishing: 238] [Article Influence: 72.0] [Reference Citation Analysis]
15 Jia X, Xu G, Du Z, Fu Y. Cu(BTC)-MOF catalyzed multicomponent reaction to construct 1,4-disubstituted-1,2,3-triazoles. Polyhedron 2018;151:515-9. [DOI: 10.1016/j.poly.2018.05.058] [Cited by in Crossref: 14] [Cited by in F6Publishing: 5] [Article Influence: 3.5] [Reference Citation Analysis]
16 Shi Y, Li M, Zhang F, Chen B. Nickel( ii )-catalyzed tandem C(sp 2 )–H bond activation and annulation of arenes with gem -dibromoalkenes. RSC Adv 2018;8:28668-75. [DOI: 10.1039/c8ra03278e] [Cited by in Crossref: 4] [Article Influence: 1.0] [Reference Citation Analysis]
17 Reddy RJ, Shankar A, Kumari AH. An Efficient Sequential One‐Pot Approach for the Synthesis of C3‐Functionalized Imidazo[1,2‐ a ]pyridines under Transition‐Metal Free Conditions. Asian J Org Chem 2019;8:2269-75. [DOI: 10.1002/ajoc.201900606] [Cited by in Crossref: 11] [Article Influence: 3.7] [Reference Citation Analysis]
18 Aksenov NA, Aksenov AV, Nadein ON, Aksenov DA, Smirnov AN, Rubin M. One-pot synthesis of benzoxazoles via the metal-free ortho-C–H functionalization of phenols with nitroalkanes. RSC Adv 2015;5:71620-6. [DOI: 10.1039/c5ra15128g] [Cited by in Crossref: 32] [Article Influence: 4.6] [Reference Citation Analysis]
19 Hou Y, Zhu L, Li Z, Shen Q, Xu Q, Li W, Liu Y, Gong P. Design, synthesis and biological evaluation of novel 7-amino-[1,2,4]triazolo[4,3-f]pteridinone, and 7-aminotetrazolo[1,5-f]pteridinone derivative as potent antitumor agents. Eur J Med Chem 2019;163:690-709. [PMID: 30572179 DOI: 10.1016/j.ejmech.2018.12.009] [Cited by in Crossref: 23] [Cited by in F6Publishing: 13] [Article Influence: 5.8] [Reference Citation Analysis]
20 Chen K, Barve IJ, Sun C. Catalyst-Controlled Regioselective Synthesis of Benzotriazlolodiazepin-7-ones and Benzotriazolodiazocin-8-ones. Org Lett 2020;22:428-32. [DOI: 10.1021/acs.orglett.9b04162] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 1.7] [Reference Citation Analysis]
21 Zaki M, Oukhrib A, El Hakmaoui A, Hiebel M, Berteina-raboin S, Akssira M. Synthesis of novel 1,2,3-triazole-substituted tomentosins. Zeitschrift für Naturforschung B 2019;74:273-81. [DOI: 10.1515/znb-2018-0225] [Cited by in Crossref: 3] [Article Influence: 1.0] [Reference Citation Analysis]
22 Chung S, Chandra P, Koo JP, Shim YB. Development of a bifunctional nanobiosensor for screening and detection of chemokine ligand in colorectal cancer cell line. Biosens Bioelectron 2018;100:396-403. [PMID: 28954256 DOI: 10.1016/j.bios.2017.09.031] [Cited by in Crossref: 21] [Cited by in F6Publishing: 14] [Article Influence: 4.2] [Reference Citation Analysis]
23 Chen Z, Zhang S, Zhang J, Zhu Z. Enhanced anti-cancer efficacy to cancer cells by a novel monofunctional mononuclear platinum( ii ) complex containing a mixed S,N,S-donor ligand. New J Chem 2017;41:6760-8. [DOI: 10.1039/c7nj01472d] [Cited by in Crossref: 6] [Article Influence: 1.2] [Reference Citation Analysis]
24 Ghoshal T, Patel TM. Anticancer activity of benzoxazole derivative (2015 onwards): a review. Futur J Pharm Sci 2020;6. [DOI: 10.1186/s43094-020-00115-0] [Cited by in Crossref: 7] [Cited by in F6Publishing: 2] [Article Influence: 3.5] [Reference Citation Analysis]