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For: Prakash O, Hussain K, Kumar R, Wadhwa D, Sharma C, Aneja KR. Synthesis and antimicrobial evaluation of new 1,4-dihydro-4-pyrazolylpyridines and 4-pyrazolylpyridines. Org Med Chem Lett 2011;1:5. [PMID: 22373350 DOI: 10.1186/2191-2858-1-5] [Cited by in Crossref: 9] [Cited by in F6Publishing: 5] [Article Influence: 0.8] [Reference Citation Analysis]
Number Citing Articles
1 El-sawy E, Ebaid M, Abo-salem H, Al-sehemi A, Mandour A. Synthesis, anti-inflammatory, analgesic and anticonvulsant activities of some new 4,6-dimethoxy-5-(heterocycles)benzofuran starting from naturally occurring visnagin. Arabian Journal of Chemistry 2014;7:914-23. [DOI: 10.1016/j.arabjc.2012.12.041] [Cited by in Crossref: 25] [Cited by in F6Publishing: 10] [Article Influence: 3.1] [Reference Citation Analysis]
2 Rao KS, Ramesh P, Trivedi R, Kantam ML. Chiral squaramide catalyzed synthesis of C4 substituted chiral pyrazol-3-ol derivatives via a facile asymmetric Michael addition of 3-methyl-2-pyrazolin-5-one to β-nitrostyrenes. Tetrahedron Letters 2016;57:1227-31. [DOI: 10.1016/j.tetlet.2016.02.008] [Cited by in Crossref: 17] [Cited by in F6Publishing: 13] [Article Influence: 2.8] [Reference Citation Analysis]
3 Khloya P, Kumar P, Mittal A, Aggarwal NK, Sharma PK. Synthesis of some novel 4-arylidene pyrazoles as potential antimicrobial agents. Org Med Chem Lett 2013;3:9. [PMID: 23981685 DOI: 10.1186/2191-2858-3-9] [Cited by in Crossref: 23] [Cited by in F6Publishing: 16] [Article Influence: 2.6] [Reference Citation Analysis]
4 Saputo S, Faustoferri RC, Quivey RG Jr. A Drug Repositioning Approach Reveals that Streptococcus mutans Is Susceptible to a Diverse Range of Established Antimicrobials and Nonantibiotics. Antimicrob Agents Chemother 2018;62:e01674-17. [PMID: 29061736 DOI: 10.1128/AAC.01674-17] [Cited by in Crossref: 7] [Cited by in F6Publishing: 10] [Article Influence: 1.4] [Reference Citation Analysis]
5 Kumar P, Kumar A, Hussain K. Iodobenzene diacetate (IBD) catalyzed an quick oxidative aromatization of Hantzsch-1,4-dihydropyridines to pyridines under ultrasonic irradiation. Ultrasonics Sonochemistry 2012;19:729-35. [DOI: 10.1016/j.ultsonch.2011.12.021] [Cited by in Crossref: 11] [Cited by in F6Publishing: 8] [Article Influence: 1.1] [Reference Citation Analysis]
6 Gholami Dehbalaei M, Foroughifar N, Khajeh-amiri A, Pasdar H. N -propylbenzoguanamine sulfonic acid-functionalized magnetic nanoparticles: A novel and magnetically retrievable catalyst for the synthesis of 1,4-dihydropyridine derivatives. J Chin Chem Soc 2018;65:1356-69. [DOI: 10.1002/jccs.201800120] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 1.3] [Reference Citation Analysis]
7 Sudhana SM, Adi PJ. Synthesis, Biological Evaluation and Molecular Docking Studies of Novel Di-hydropyridine Analogs as Potent Antioxidants. Curr Top Med Chem 2019;19:2676-86. [PMID: 31702500 DOI: 10.2174/1568026619666191105100959] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.7] [Reference Citation Analysis]