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For: Jampilek J. Heterocycles in Medicinal Chemistry. Molecules 2019;24:E3839. [PMID: 31731387 DOI: 10.3390/molecules24213839] [Cited by in Crossref: 52] [Cited by in F6Publishing: 21] [Article Influence: 17.3] [Reference Citation Analysis]
Number Citing Articles
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2 Shishkina SV, Konovalova IS, Karpina VR, Kovalenko SS, Kovalenko SM, Bunyatyan ND. Concomitant polymorphic forms of 3-cyclopropyl-5-(2-hydrazinylpyridin-3-yl)-1,2,4-oxadiazole. Acta Crystallogr C Struct Chem 2020;76:836-44. [DOI: 10.1107/s2053229620010414] [Cited by in Crossref: 2] [Article Influence: 1.0] [Reference Citation Analysis]
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4 Nan J, Ma Q, Yin J, Liang C, Tian L, Ma Y. Rh III -Catalyzed formal [5 + 1] cyclization of 2-pyrrolyl/indolylanilines using vinylene carbonate as a C1 synthon. Org Chem Front 2021;8:1764-9. [DOI: 10.1039/d1qo00040c] [Cited by in Crossref: 8] [Article Influence: 8.0] [Reference Citation Analysis]
5 Li Petri G, Raimondi MV, Spanò V, Holl R, Barraja P, Montalbano A. Pyrrolidine in Drug Discovery: A Versatile Scaffold for Novel Biologically Active Compounds. Top Curr Chem (Cham) 2021;379:34. [PMID: 34373963 DOI: 10.1007/s41061-021-00347-5] [Reference Citation Analysis]
6 Mekonnen Sanka B, Mamo Tadesse D, Teju Bedada E, Mengesha ET, Babu G N. Design, synthesis, biological screening and molecular docking studies of novel multifunctional 1,4-di (aryl/heteroaryl) substituted piperazine derivatives as potential antitubercular and antimicrobial agents. Bioorg Chem 2021;119:105568. [PMID: 34968884 DOI: 10.1016/j.bioorg.2021.105568] [Reference Citation Analysis]
7 Long Ngo H, Kumar Mishra D, Mishra V, Chien Truong C. Recent advances in the synthesis of heterocycles and pharmaceuticals from the photo/electrochemical fixation of carbon dioxide. Chemical Engineering Science 2021;229:116142. [DOI: 10.1016/j.ces.2020.116142] [Cited by in Crossref: 5] [Cited by in F6Publishing: 1] [Article Influence: 5.0] [Reference Citation Analysis]
8 Davenel V, Nisole C, Fontaine-Vive F, Fourquez JM, Chollet AM, Michelet V. Gold-Catalyzed Cycloisomerization of 1,6-Cyclohexenylalkyne: An Efficient Entry to Bicyclo[3.2.1]oct-2-ene and Bicyclo[3.3.1]nonadiene. J Org Chem 2020;85:12657-69. [PMID: 32875797 DOI: 10.1021/acs.joc.0c01841] [Cited by in Crossref: 4] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
9 Ojha B, Laxman K, Ravikanth M. Crowned Macrocycles Containing Two Pyrrolo[1,2-a] Indoles Created By Intramolecular Fusion. Chem Asian J 2021;16:3221-9. [PMID: 34405967 DOI: 10.1002/asia.202100799] [Reference Citation Analysis]
10 Correia JTM, Santos MS, Pissinati EF, da Silva GP, Paixão MW. Recent Advances on Photoinduced Cascade Strategies for the Synthesis of N-Heterocycles. Chem Rec 2021;21:2666-87. [PMID: 34288377 DOI: 10.1002/tcr.202100160] [Reference Citation Analysis]
11 Ettaoussi M, Laversin A, Vreulz B, Rami M, Lebegue N, Delagrange P, Caignard DH, Melnyk P, Liberelle M, Yous S. Synthesis and SAR Studies of Isoquinoline and Tetrahydroisoquinoline Derivatives as Melatonin Receptor Ligands. ChemMedChem 2021. [PMID: 34797951 DOI: 10.1002/cmdc.202100658] [Reference Citation Analysis]
12 Alshammari MM, Soury R, Alenezi KM, Mushtque M, Rizvi MMA, Haque A. Synthesis, characterization, anticancer and in silico studies of a pyrazole-tethered thiazolidine-2,4-dione derivative. J Biomol Struct Dyn 2021;:1-8. [PMID: 34551668 DOI: 10.1080/07391102.2021.1981451] [Reference Citation Analysis]
13 Benassi A, Doria F, Pirota V. Groundbreaking Anticancer Activity of Highly Diversified Oxadiazole Scaffolds. Int J Mol Sci 2020;21:E8692. [PMID: 33217987 DOI: 10.3390/ijms21228692] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 3.5] [Reference Citation Analysis]
14 Bąchor U, Mączyński M. Selected β2-, β3- and β2,3-Amino Acid Heterocyclic Derivatives and Their Biological Perspective. Molecules 2021;26:438. [PMID: 33467741 DOI: 10.3390/molecules26020438] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
15 Kassel VM, Hanneman CM, Delaney CP, Denmark SE. Heteroaryl-Heteroaryl, Suzuki-Miyaura, Anhydrous Cross-Coupling Reactions Enabled by Trimethyl Borate. J Am Chem Soc 2021;143:13845-53. [PMID: 34415757 DOI: 10.1021/jacs.1c06419] [Reference Citation Analysis]
16 Qiu ZX, Dong PZ, Zhao HL, Zhao MF, Qiu B, Xiao J. Brønsted Acid-Catalyzed Minisci-Type Cross-Dehydrogenative Coupling of N-Heteroaromatics and Cyclic Ethers. J Org Chem 2021;86:9299-305. [PMID: 34181422 DOI: 10.1021/acs.joc.1c00337] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
17 Gaweda K, Plazinska A, Plazinski W. Conformations of saturated five-membered heterocycles evaluated by MP2 calculations. Chem Heterocycl Comp 2020;56:1599-604. [DOI: 10.1007/s10593-020-02855-6] [Cited by in Crossref: 4] [Article Influence: 4.0] [Reference Citation Analysis]
18 Cantini N, Khlebnikov AI, Crocetti L, Schepetkin IA, Floresta G, Guerrini G, Vergelli C, Bartolucci G, Quinn MT, Giovannoni MP. Exploration of nitrogen heterocycle scaffolds for the development of potent human neutrophil elastase inhibitors. Bioorg Med Chem 2021;29:115836. [PMID: 33218895 DOI: 10.1016/j.bmc.2020.115836] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
19 Ali AAA, Lee Y, Wu AT, Yadav VK, Yu D, Huang H. Structure-based strategies for synthesis, lead optimization and biological evaluation of N-substituted anthra[1,2-c][1,2,5]thiadiazole-6,11-dione derivatives as potential multi-target anticancer agents. Arabian Journal of Chemistry 2021;14:102884. [DOI: 10.1016/j.arabjc.2020.10.031] [Cited by in Crossref: 4] [Cited by in F6Publishing: 1] [Article Influence: 4.0] [Reference Citation Analysis]
20 Wang S, Yuan XH, Wang SQ, Zhao W, Chen XB, Yu B. FDA-approved pyrimidine-fused bicyclic heterocycles for cancer therapy: Synthesis and clinical application. Eur J Med Chem 2021;214:113218. [PMID: 33540357 DOI: 10.1016/j.ejmech.2021.113218] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
21 Paris TJ, Schwartz C, Willand-Charnley R. Electrophilic Etherification of α-Heteroaryl Carbanions with Monoperoxyacetals as a Route to Ketene O,O- and N,O-Acetals. J Org Chem 2021;86:2369-84. [PMID: 33464889 DOI: 10.1021/acs.joc.0c02506] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
22 Prusty N, Banjare SK, Mohanty SR, Nanda T, Yadav K, Ravikumar PC. Synthesis and Photophysical Study of Heteropolycyclic and Carbazole Motif: Nickel-Catalyzed Chelate-Assisted Cascade C-H Activations/Annulations. Org Lett 2021;23:9041-6. [PMID: 34788053 DOI: 10.1021/acs.orglett.1c03234] [Reference Citation Analysis]
23 Jain A, Chaudhary J, Khaira H, Chopra B, Dhingra A. Piperazine: A Promising Scaffold with Analgesic and Anti-inflammatory Potential. Drug Res (Stuttg) 2021;71:62-72. [PMID: 33336346 DOI: 10.1055/a-1323-2813] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
24 Elhalem E, Bellomo A, Cooke M, Scravaglieri A, Pearce LV, Peach ML, Gandolfi Donadío L, Kazanietz MG, Comin MJ. Design, Synthesis, and Characterization of Novel sn-1 Heterocyclic DAG-Lactones as PKC Activators. J Med Chem 2021;64:11418-31. [PMID: 34279947 DOI: 10.1021/acs.jmedchem.1c00739] [Reference Citation Analysis]
25 Viveki AB, Pol MD, Halder P, Sonavane SR, Mhaske SB. Annulation of Enals with Carbamoylpropiolates via NHC-Catalyzed Enolate Pathway: Access to Functionalized Maleimides/Iso-maleimides and Synthesis of Aspergillus FH-X-213. J Org Chem 2021;86:9466-77. [PMID: 34213335 DOI: 10.1021/acs.joc.1c00782] [Reference Citation Analysis]
26 Ganta RK, Kerru N, Maddila S, Jonnalagadda SB. Advances in Pyranopyrazole Scaffolds' Syntheses Using Sustainable Catalysts-A Review. Molecules 2021;26:3270. [PMID: 34071629 DOI: 10.3390/molecules26113270] [Reference Citation Analysis]
27 Majumder S, Ghosh S, Pyne P, Ghosh A, Ghosh D, Hajra A. Synthesis of Unsymmetrical Biheteroarenes via Dehydrogenative and Decarboxylative Coupling: a Decade Update. Chem Rec 2021;:e202100288. [PMID: 34970849 DOI: 10.1002/tcr.202100288] [Reference Citation Analysis]
28 Palani V, Perea MA, Sarpong R. Site-Selective Cross-Coupling of Polyhalogenated Arenes and Heteroarenes with Identical Halogen Groups. Chem Rev 2021. [PMID: 34402611 DOI: 10.1021/acs.chemrev.1c00513] [Reference Citation Analysis]
29 Vega Alanis BA, Iorio MT, Silva LL, Bampali K, Ernst M, Schnürch M, Mihovilovic MD. Allosteric GABAA Receptor Modulators-A Review on the Most Recent Heterocyclic Chemotypes and Their Synthetic Accessibility. Molecules 2020;25:E999. [PMID: 32102309 DOI: 10.3390/molecules25040999] [Cited by in Crossref: 8] [Cited by in F6Publishing: 6] [Article Influence: 4.0] [Reference Citation Analysis]
30 Rashid HU, Martines MAU, Duarte AP, Jorge J, Rasool S, Muhammad R, Ahmad N, Umar MN. Research developments in the syntheses, anti-inflammatory activities and structure–activity relationships of pyrimidines. RSC Adv 2021;11:6060-98. [DOI: 10.1039/d0ra10657g] [Cited by in Crossref: 5] [Article Influence: 5.0] [Reference Citation Analysis]
31 Hariri M, Darvish F, Mengue Me Ndong KP, Sechet N, Chacktas G, Boosaliki H, Tran Do ML, Mwande-Maguene G, Lebibi J, Burilov AR, Ayad T, Virieux D, Pirat JL. Gold-Catalyzed Access to Isophosphinoline 2-Oxides. J Org Chem 2021;86:7813-24. [PMID: 34009995 DOI: 10.1021/acs.joc.1c00648] [Reference Citation Analysis]
32 Cortes Vazquez J, Davis J, Nesterov VN, Wang H, Luo W. Sc(OTf)3-Catalyzed Formal [3 + 3] Cycloaddition Reaction of Diaziridines and Quinones for the Synthesis of Benzo[e][1,3,4]oxadiazines. Org Lett 2021;23:3136-40. [PMID: 33819425 DOI: 10.1021/acs.orglett.1c00818] [Reference Citation Analysis]