BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Nehra B, Rulhania S, Jaswal S, Kumar B, Singh G, Monga V. Recent advancements in the development of bioactive pyrazoline derivatives. Eur J Med Chem 2020;205:112666. [PMID: 32795767 DOI: 10.1016/j.ejmech.2020.112666] [Cited by in Crossref: 12] [Cited by in F6Publishing: 5] [Article Influence: 6.0] [Reference Citation Analysis]
Number Citing Articles
1 Rajamanickam R, Sivakolunthu S, Sampathkumar J. Synthesis, crystal structure, Hirshfeld surface, DFT and docking studies of 4-[(5‑hydroxy-3-methyl-1-phenyl-1H-pyrazol-4-yl)(phenyl)methyl]-5-methyl-2-phenyl-1,2-dihydro-3H-pyrazol-3-one. Journal of Molecular Structure 2022;1252:132170. [DOI: 10.1016/j.molstruc.2021.132170] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
2 Farooq S, Ngaini Z. Microwave‐Assisted Synthesis, Antimicrobial Activities and Molecular Docking of Methoxycarboxylated Chalcone Derived Pyrazoline and Pyrazole Derivatives. ChemistrySelect 2022;7. [DOI: 10.1002/slct.202103984] [Reference Citation Analysis]
3 Slivka M, Korol N. Synthesis of mononuclear heterocycles via electrophilic cyclization. Monatsh Chem 2022;153:1-8. [DOI: 10.1007/s00706-021-02869-6] [Reference Citation Analysis]
4 Wen K, Wu Y, Chen J, Shi J, Zheng M, Yao X, Tang X. Copper-Mediated Decarboxylative Coupling of 3-Indoleacetic Acids with Pyrazolones. ACS Omega 2022;7:5274-82. [PMID: 35187342 DOI: 10.1021/acsomega.1c06443] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
5 Yavari MA, Taslimi P, Bayrak C, Taskin‐tok T, Menzek A. 1, 3‐dipolar cycloaddition reactions of the compound obtaining from cyclopentadiene‐PTAD and biological activities of adducts formed selectively. Journal of Heterocyclic Chem. [DOI: 10.1002/jhet.4426] [Reference Citation Analysis]
6 Sever B, Altıntop MD, Demir Y, Yılmaz N, Akalın Çiftçi G, Beydemir Ş, Özdemir A. Identification of a new class of potent aldose reductase inhibitors: Design, microwave-assisted synthesis, in vitro and in silico evaluation of 2-pyrazolines. Chem Biol Interact 2021;345:109576. [PMID: 34252406 DOI: 10.1016/j.cbi.2021.109576] [Reference Citation Analysis]
7 Zhang J, Li X, Wei H, Li Y, Zhang G, Li Y. Sequential DNA-Encoded Building Block Fusion for the Construction of Polysubstituted Pyrazoline Core Libraries. Org Lett 2021;23:8429-33. [PMID: 34652930 DOI: 10.1021/acs.orglett.1c03145] [Reference Citation Analysis]
8 Chen J, Liu N, Hu Q, Liu J, Wu J, Cai Q, Wu J. Photocatalytic three-component radical cascade: a general route to heterocyclic-substituted alkyl sulfones. Org Chem Front 2021;8:5316-21. [DOI: 10.1039/d1qo00957e] [Cited by in Crossref: 9] [Cited by in F6Publishing: 8] [Article Influence: 9.0] [Reference Citation Analysis]
9 Singh G, Kajal K, Pradhan T, Bhurta D, Monga V. The medicinal perspective of 2,4-thiazolidinediones based ligands as antimicrobial, antitumor and antidiabetic agents: A review. Arch Pharm (Weinheim) 2022;:e2100517. [PMID: 35715383 DOI: 10.1002/ardp.202100517] [Reference Citation Analysis]
10 Wang Y, Shi W, Wu C, Wan L, Zhao Y, Zhang C, Gu W, Wang S. Pyrazole ring-containing isolongifolanone derivatives as potential CDK2 inhibitors: Evaluation of anticancer activity and investigation of action mechanism. Biomed Pharmacother 2021;139:111663. [PMID: 34243605 DOI: 10.1016/j.biopha.2021.111663] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
11 Dhameliya TM, Bhakhar KA, Gajjar ND, Patel KA, Devani AA, Hirani RV. Recent advancements and developments in search of anti-tuberculosis agents: A quinquennial update and future directions. Journal of Molecular Structure 2022;1248:131473. [DOI: 10.1016/j.molstruc.2021.131473] [Cited by in Crossref: 10] [Cited by in F6Publishing: 7] [Article Influence: 10.0] [Reference Citation Analysis]
12 Mehmood R, Sadiq A, Alsantali RI, Mughal EU, Alsharif MA, Naeem N, Javid A, Al-Rooqi MM, Chaudhry GE, Ahmed SA. Synthesis and Evaluation of 1,3,5-Triaryl-2-Pyrazoline Derivatives as Potent Dual Inhibitors of Urease and α-Glucosidase Together with Their Cytotoxic, Molecular Modeling and Drug-Likeness Studies. ACS Omega 2022;7:3775-95. [PMID: 35128286 DOI: 10.1021/acsomega.1c06694] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 4.0] [Reference Citation Analysis]
13 Vahedpour T, Hamzeh‐mivehroud M, Hemmati S, Dastmalchi S. Synthesis of 2‐Pyrazolines from Hydrazines: Mechanisms Explained. ChemistrySelect 2021;6:6483-506. [DOI: 10.1002/slct.202101467] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
14 Wang S, Sun L, Gao M, Jiang Q, Hu W, Liu Y, Tao C. Copper-catalyzed C2 alkenylation of pyridine-N-oxides with alkynes. Chem Commun (Camb) 2022;58:7168-71. [PMID: 35670310 DOI: 10.1039/d2cc00851c] [Reference Citation Analysis]
15 Haider K, Sharma S, Pokharel YR, Das S, Joseph A, Najmi AK, Ahmad F, Yar MS. Synthesis, biological evaluation, and in silico studies of indole-tethered pyrazoline derivatives as anticancer agents targeting topoisomerase IIα. Drug Dev Res 2022. [PMID: 35898169 DOI: 10.1002/ddr.21976] [Reference Citation Analysis]
16 Song Z, Zhu K, Jiang H, Gong H, Ye Z, Zhang F. Synthesis of 1,3-Dioxepine-Fused (Tricyclic) Bispyrazoles Involved with Pyrazolone Derivatives and Dichloromethane. J Org Chem 2022. [PMID: 35262363 DOI: 10.1021/acs.joc.1c03121] [Reference Citation Analysis]
17 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: 4] [Article Influence: 5.0] [Reference Citation Analysis]
18 Popova SA, Pavlova EV, Shevchenko OG, Chukicheva IY, Kutchin AV. Isobornylchalcones as Scaffold for the Synthesis of Diarylpyrazolines with Antioxidant Activity. Molecules 2021;26:3579. [PMID: 34208180 DOI: 10.3390/molecules26123579] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
19 Shawish I, Barakat A, Aldalbahi A, Malebari AM, Nafie MS, Bekhit AA, Albohy A, Khan A, Ul-haq Z, Haukka M, de la Torre BG, Albericio F, El-faham A. Synthesis and Antiproliferative Activity of a New Series of Mono- and Bis(dimethylpyrazolyl)- s -triazine Derivatives Targeting EGFR/PI3K/AKT/mTOR Signaling Cascades. ACS Omega. [DOI: 10.1021/acsomega.2c03079] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
20 Chang J, Yao Y, Xia Y, Liu L, Zhang Y. Preparation of 5-methyl-3,5-dipropyl-2-pyrazoline catalyzed by chloroaluminate ionic liquids. Journal of Molecular Structure 2022;1256:132539. [DOI: 10.1016/j.molstruc.2022.132539] [Reference Citation Analysis]
21 Rana M, Faizan MI, Dar SH, Ahmad T, Rahisuddin. Design and Synthesis of Carbothioamide/Carboxamide-Based Pyrazoline Analogs as Potential Anticancer Agents: Apoptosis, Molecular Docking, ADME Assay, and DNA Binding Studies. ACS Omega. [DOI: 10.1021/acsomega.2c02033] [Reference Citation Analysis]
22 Haider K, Shafeeque M, Yahya S, Yar MS. A comprehensive review on pyrazoline based heterocyclic hybrids as potent anticancer agents. European Journal of Medicinal Chemistry Reports 2022;5:100042. [DOI: 10.1016/j.ejmcr.2022.100042] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
23 Bahadur A, Iqbal S, Ujan R, Channar PA, Al-Anazy MM, Saeed A, Mahmood Q, Shoaib M, Shah M, Arshad I, Shabir G, Saifullah M, Liu G, Qayyum MA. Effect of organic solvents on solvatochromic, fluorescence, and electrochemical properties of synthesized thiazolylcoumarin derivatives. Luminescence 2021;36:1189-97. [PMID: 33759314 DOI: 10.1002/bio.4044] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
24 Wang Q, Wang L, Pajkert R, Hajdin I, Mei H, Röschenthaler G, Han J. [3+2] Cycloaddition reactions of β-diazo-α,α-difluoromethylphosphonates with α,β-unsaturated esters. Journal of Fluorine Chemistry 2021;251:109899. [DOI: 10.1016/j.jfluchem.2021.109899] [Reference Citation Analysis]
25 Adam AMA, Altalhi TA, Saad HA, Refat MS, Hegab MS. Exploring the charge-transfer chemistry of fluorine-containing pyrazolin-5-ones: The complexation of 1-methyl-3-trifluoromethyl-2-pyrazoline-5-one with five π-acceptors. Journal of Molecular Liquids 2021;331:115814. [DOI: 10.1016/j.molliq.2021.115814] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 4.0] [Reference Citation Analysis]