{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,3]],"date-time":"2026-07-03T16:48:29Z","timestamp":1783097309050,"version":"3.54.6"},"reference-count":53,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2018,12,13]],"date-time":"2018-12-13T00:00:00Z","timestamp":1544659200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"name":"Research Council of Shahrood University of Technology"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Chemistry &amp; Biodiversity"],"published-print":{"date-parts":[[2019,1]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>The salophen copper(II) complex was successfully used for the efficient synthesis of new 1,2,3\u2010triazoles based on the naphthalene\u20101,4\u2010dione scaffold. The reaction of 2\u2010chloro\u20103\u2010(prop\u20102\u2010yn\u20101\u2010yloxy)naphthalene\u20101,4\u2010dione or 2,3\u2010bis(prop\u20102\u2010yn\u20101\u2010yloxy)naphthalene\u20101,4\u2010dione with aromatic azides in the presence of a low copper catalyst (loading 1\u2005mol\u2010%) afforded 2\u2010chloro\u20103\u2010[(1\u2010phenyl\u20101<jats:italic>H<\/jats:italic>\u20101,2,3\u2010triazol\u20104\u2010yl)methoxy]naphthalene\u20101,4\u2010dione or 2,3\u2010bis[(1\u2010phenyl\u20101<jats:italic>H<\/jats:italic>\u20101,2,3\u2010triazol\u20104\u2010yl)methoxy]naphthalene\u20101,4\u2010dione, respectively. The advantages of these reactions are short reaction times, high\u2010to\u2010excellent reaction yields, operational simplicity, and mild experimental conditions. The new 1,2,3\u2010triazoles obtained were screened for their <jats:italic>in\u2005vitro<\/jats:italic> antibacterial activities and were subjected to molecular docking studies.<\/jats:p>","DOI":"10.1002\/cbdv.201800410","type":"journal-article","created":{"date-parts":[[2018,10,20]],"date-time":"2018-10-20T17:59:02Z","timestamp":1540058342000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":18,"title":["Salophen Copper(II) Complex\u2010Assisted Click Reactions for Fast Synthesis of 1,2,3\u2010Triazoles Based on Naphthalene\u20101,4\u2010dione Scaffold, Antibacterial Evaluation, and Molecular Docking Studies"],"prefix":"10.1002","volume":"16","author":[{"given":"Sima","family":"Abbaspour","sequence":"first","affiliation":[{"name":"Faculty of Chemistry Shahrood University of Technology  Shahrood 36199-95161 Iran"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-1430-7399","authenticated-orcid":false,"given":"Ali","family":"Keivanloo","sequence":"additional","affiliation":[{"name":"Faculty of Chemistry Shahrood University of Technology  Shahrood 36199-95161 Iran"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mohammad","family":"Bakherad","sequence":"additional","affiliation":[{"name":"Faculty of Chemistry Shahrood University of Technology  Shahrood 36199-95161 Iran"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Saghi","family":"Sepehri","sequence":"additional","affiliation":[{"name":"Department of Medicinal Chemistry, School of Pharmacy, Ardabil University of Medical Sciences  Ardabil 56189-53142 Iran"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2018,12,13]]},"reference":[{"key":"e_1_2_7_1_1","doi-asserted-by":"crossref","unstructured":"W. Shi C. Liu A. Lei \u2018Transition-metal catalyzed oxidative cross-coupling reactions to form C\u2212C bonds involving organometallic reagents as nucleophiles\u2019 Chem. Soc. Rev.2011 40 2761\u20132776.","DOI":"10.1039\/c0cs00125b"},{"key":"e_1_2_7_2_1","doi-asserted-by":"crossref","unstructured":"I.\u2005P. Beletskaya A.\u2005V. Cheprakov \u2018Copper in cross-coupling reactions: the post-Ullmann chemistry\u2019 Coord. Chem. Rev.2004 248 2337\u20132364.","DOI":"10.1016\/j.ccr.2004.09.014"},{"key":"e_1_2_7_3_1","doi-asserted-by":"crossref","unstructured":"S.\u2005G. Agalave S.\u2005R. Maujan V.\u2005S. Pore \u2018Click chemistry: 1 2 3-triazoles as pharmacophores\u2019 Chem. Asian J.2011 6 2696\u20132718.","DOI":"10.1002\/asia.201100432"},{"key":"e_1_2_7_4_1","doi-asserted-by":"crossref","unstructured":"M. Meldal C.\u2005W. Torn\u00f8e \u2018Cu-catalyzed azide-alkyne cycloaddition\u2019 Chem. Rev.2008 108 2952\u20133015.","DOI":"10.1021\/cr0783479"},{"key":"e_1_2_7_5_1","doi-asserted-by":"crossref","unstructured":"V.\u2005V. Rostovtsev L.\u2005G. Green V.\u2005V. Fokin K.\u2005B. Sharpless \u2018A Stepwise Huisgen Cycloaddition Process: Copper(I)-Catalyzed Regioselective \u201cLigation\u201d of Azides and Terminal Alkynes\u2019 Angew. Chem.2002 114 2708\u20132711.","DOI":"10.1002\/1521-3757(20020715)114:14<2708::AID-ANGE2708>3.0.CO;2-0"},{"key":"e_1_2_7_6_1","doi-asserted-by":"crossref","unstructured":"C.\u2005W. Torn\u00f8e C. Christensen M. Meldal \u2018Peptidotriazoles on solid phase:[1 2 3]-triazoles by regiospecific copper (I)-catalyzed 1 3-dipolar cycloadditions of terminal alkynes to azides\u2019 J. Org. Chem.2002 67 3057\u20133064.","DOI":"10.1021\/jo011148j"},{"key":"e_1_2_7_7_1","doi-asserted-by":"crossref","unstructured":"J.\u2005M. Baskin C.\u2005R. Bertozzi \u2018Copper-Free Click Chemistry: Bioorthogonal Reagents for Tagging Azides\u2019 Aldrichimica Acta2010 43 15\u201323.","DOI":"10.1002\/chin.201124237"},{"key":"e_1_2_7_8_1","doi-asserted-by":"crossref","unstructured":"1 5-Disubstituted triazoles can be regioselectively prepared with ruthenium catalysis although under non-click conditions: B.\u2005C. Boren S. Narayan L.\u2005K. Rasmussen L. Zhang H. Zhao Z. Lin G. Jia V.\u2005V. Fokin \u2018Ruthenium-catalyzed azide-alkyne cycloaddition: Scope and mechanism\u2019 J. Am. Chem. Soc.2008 130 8923\u20138930.","DOI":"10.1021\/ja0749993"},{"key":"e_1_2_7_9_1","doi-asserted-by":"crossref","unstructured":"G.-C. Kuang H.\u2005A. Michaels J.\u2005T. Simmons R.\u2005J. Clark L. Zhu \u2018Chelation-assisted copper (II)-acetate-accelerated azide-alkyne cycloaddition\u2019 J. Org. Chem.2010 75 6540\u20136548.","DOI":"10.1021\/jo101305m"},{"key":"e_1_2_7_10_1","doi-asserted-by":"crossref","unstructured":"V.\u2005O. Rodionov S.\u2005I. Presolski S. Gardinier Y.-H. Lim M. Finn \u2018Benzimidazole and related ligands for Cu-catalyzed azide-alkyne cycloaddition\u2019 J. Am. Chem. Soc.2007 129 12696\u201312704.","DOI":"10.1021\/ja072678l"},{"key":"e_1_2_7_11_1","doi-asserted-by":"crossref","unstructured":"S.\u2005I. Presolski V. Hong S.-H. Cho M. Finn \u2018Tailored ligand acceleration of the Cu-catalyzed azide-alkyne cycloaddition reaction: practical and mechanistic implications\u2019 J. Am. Chem. Soc.2010 132 14570\u201314576.","DOI":"10.1021\/ja105743g"},{"key":"e_1_2_7_12_1","doi-asserted-by":"crossref","unstructured":"T.\u2005R. Chan R. Hilgraf K.\u2005B. Sharpless V.\u2005V. Fokin \u2018Polytriazoles as copper (I)-stabilizing ligands in catalysis\u2019 Org. Lett.2004 6 2853\u20132855.","DOI":"10.1021\/ol0493094"},{"key":"e_1_2_7_13_1","doi-asserted-by":"crossref","unstructured":"J.\u2005E. Hein V.\u2005V. Fokin \u2018Copper-catalyzed azide\u2013alkyne cycloaddition (CuAAC) and beyond: new reactivity of copper (I) acetylides\u2019 Chem. Soc. Rev.2010 39 1302\u20131315.","DOI":"10.1039\/b904091a"},{"key":"e_1_2_7_14_1","doi-asserted-by":"crossref","unstructured":"H.\u2005A. Michaels L. Zhu \u2018Ligand-Assisted Copper (II) Acetate-Accelerated Azide\u2013Alkyne Cycloaddition\u2019 Chem. Asian J.2011 6 2825\u20132834.","DOI":"10.1002\/asia.201100426"},{"key":"e_1_2_7_15_1","doi-asserted-by":"crossref","unstructured":"N. Candelon D. Last\u00e9cou\u00e8res A.\u2005K. Diallo J.\u2005R. Aranzaes D. Astruc J.-M. Vincent \u2018A highly active and reusable copper (I)-tren catalyst for the \u201cclick\u201d 1 3-dipolar cycloaddition of azides and alkynes\u2019 Chem. Commun.2008 741\u2013743.","DOI":"10.1039\/B716306A"},{"key":"e_1_2_7_16_1","doi-asserted-by":"crossref","unstructured":"S. Narayan J. Muldoon M. Finn V.\u2005V. Fokin H.\u2005C. Kolb K.\u2005B. Sharpless \u2018\u201cOn water\u201d: Unique reactivity of organic compounds in aqueous suspension\u2019 Angew. Chem. Int. Ed.2005 44 3275\u20133279.","DOI":"10.1002\/anie.200462883"},{"key":"e_1_2_7_17_1","doi-asserted-by":"crossref","unstructured":"T. Hasegawa M. Umeda M. Numata T. Fujisawa S. Haraguchi K. Sakurai S. Shinkai \u2018Click chemistry on curdlan: a regioselective and quantitative approach to develop artificial \u03b2-1 3-glucans with various functional appendages\u2019 Chem. Lett.2005 35 82\u201383.","DOI":"10.1246\/cl.2006.82"},{"key":"e_1_2_7_18_1","doi-asserted-by":"crossref","unstructured":"S. Hartwig S. Hecht \u2018Polypseudopeptides with Variable Stereochemistry: Synthesis via Click-Chemistry Postfunctionalization and Conformational Behavior in Solution\u2019 Macromolecules2009 43 242\u2013248.","DOI":"10.1021\/ma902018w"},{"key":"e_1_2_7_19_1","doi-asserted-by":"crossref","unstructured":"A. Baron Y. Bl\u00e9riot M. Sollogoub B. Vauzeilles \u2018Phenylenediamine catalysis of \u201cclick glycosylations\u201d in water: practical and direct access to unprotected neoglycoconjugates\u2019 Org. Biomol. Chem.2008 6 1898\u20131901.","DOI":"10.1039\/b805528a"},{"key":"e_1_2_7_20_1","doi-asserted-by":"crossref","unstructured":"L. Bonami W. Van Camp D. Van Rijckegem F.\u2005E. Du\u2005Prez \u2018Facile Access to an Efficient Solid-Supported Click Catalyst System Based on Poly (ethyleneimine)\u2019 Macromol. Rapid Commun.2009 30 34\u201338.","DOI":"10.1002\/marc.200800607"},{"key":"e_1_2_7_21_1","doi-asserted-by":"crossref","unstructured":"H.\u2005C. Kolb K.\u2005B. Sharpless \u2018The growing impact of click chemistry on drug discovery\u2019 Drug Discovery Today2003 8 1128\u20131137.","DOI":"10.1016\/S1359-6446(03)02933-7"},{"key":"e_1_2_7_22_1","doi-asserted-by":"crossref","unstructured":"N.\u2005G. Aher V.\u2005S. Pore N.\u2005N. Mishra A. Kumar P.\u2005K. Shukla A. Sharma M.\u2005K. Bhat \u2018Synthesis and antifungal activity of 1 2 3-triazole containing fluconazole analogues\u2019 Bioorg. Med. Chem. Lett.2009 19 759\u2013763.","DOI":"10.1016\/j.bmcl.2008.12.026"},{"key":"e_1_2_7_23_1","doi-asserted-by":"crossref","unstructured":"J.\u2005A. Demaray J.\u2005E. Thuener M.\u2005N. Dawson S.\u2005J. Sucheck \u2018Synthesis of triazole-oxazolidinones via a one-pot reaction and evaluation of their antimicrobial activity\u2019 Bioorg. Med. Chem. Lett.2008 18 4868\u20134871.","DOI":"10.1016\/j.bmcl.2008.07.087"},{"key":"e_1_2_7_24_1","doi-asserted-by":"crossref","unstructured":"X.-L. Wang K. Wan C.-H. Zhou \u2018Synthesis of novel sulfanilamide-derived 1 2 3-triazoles and their evaluation for antibacterial and antifungal activities\u2019 Eur. J. Med. Chem.2010 45 4631\u20134639.","DOI":"10.1016\/j.ejmech.2010.07.031"},{"key":"e_1_2_7_25_1","doi-asserted-by":"crossref","unstructured":"D.\u2005R. Buckle D.\u2005J. Outred C.\u2005J. Rockell H. Smith B.\u2005A. Spicer \u2018Studies on v-triazoles. 7. Antiallergic 9-oxo-1H 9H-benzopyrano[2 3-d]-v-triazoles\u2019 J. Med. Chem.1983 26 251\u2013254.","DOI":"10.1021\/jm00356a025"},{"key":"e_1_2_7_26_1","doi-asserted-by":"crossref","unstructured":"M. Whiting J.\u2005C. Tripp Y.-C. Lin W. Lindstrom A.\u2005J. Olson J.\u2005H. Elder K.\u2005B. Sharpless V.\u2005V. Fokin \u2018Rapid Discovery and Structure\u2013Activity Profiling of Novel Inhibitors of Human Immunodeficiency Virus Type 1 Protease Enabled by the Copper(I)-Catalyzed Synthesis of 1 2 3-Triazoles and Their Further Functionalization\u2019 J. Med. Chem.2006 49 7697\u20137710.","DOI":"10.1021\/jm060754+"},{"key":"e_1_2_7_27_1","doi-asserted-by":"crossref","unstructured":"M.\u2005J. Giffin H. Heaslet A. Brik Y.-C. Lin G. Cauvi C.-H. Wong D.\u2005E. McRee J.\u2005H. Elder C.\u2005D. Stout B.\u2005E. Torbett \u2018A Copper(I)-Catalyzed 1 2 3-Triazole Azide-Alkyne Click Compound Is a Potent Inhibitor of a Multidrug-Resistant HIV-1 Protease Variant\u2019 J. Med. Chem.2008 51 6263\u20136270.","DOI":"10.1021\/jm800149m"},{"key":"e_1_2_7_28_1","doi-asserted-by":"crossref","unstructured":"M.\u2005S. Costa N. Boechat \u00c9.\u2005A. Rangel F.\u2005d.\u2005C. Da\u2005Silva A.\u2005M. de\u2005Souza C.\u2005R. Rodrigues H.\u2005C. Castro I.\u2005N. Junior M.\u2005C.\u2005S. Louren\u00e7o S.\u2005M. Wardell V.\u2005F. Ferreira \u2018Synthesis tuberculosis inhibitory activity and SAR study of N-substituted-phenyl-1 2 3-triazole derivatives\u2019 Bioorg. Med. Chem.2006 14 8644\u20138653.","DOI":"10.1016\/j.bmc.2006.08.019"},{"key":"e_1_2_7_29_1","doi-asserted-by":"crossref","unstructured":"S.\u2005R. Patpi L. Pulipati P. Yogeeswari D. Sriram N. Jain B. Sridhar R. Murthy S.\u2005V. Kalivendi S. Kantevari \u2018Design Synthesis and Structure-Activity Correlations of Novel Dibenzo[b d]furan Dibenzo[b d]thiophene andN-Methylcarbazole Clubbed 1 2 3-Triazoles as Potent Inhibitors ofMycobacterium tuberculosis\u2019 J. Med. Chem.2012 55 3911\u20133922.","DOI":"10.1021\/jm300125e"},{"key":"e_1_2_7_30_1","doi-asserted-by":"crossref","unstructured":"R. De Simone M.\u2005G. Chini I. Bruno R. Riccio D. Mueller O. Werz G. Bifulco \u2018Structure-Based Discovery of Inhibitors of Microsomal Prostaglandin E2 Synthase-1 5-Lipoxygenase and 5-Lipoxygenase-Activating Protein: Promising Hits for the Development of New Anti-inflammatory Agents\u2019 J. Med. Chem.2011 54 1565\u20131575.","DOI":"10.1021\/jm101238d"},{"key":"e_1_2_7_31_1","doi-asserted-by":"crossref","unstructured":"G.\u2005C. Brand\u00e3o F.\u2005C.\u2005R. Missias L.\u2005M. Arantes L.\u2005F. Soares K.\u2005K. Roy R.\u2005J. Doerksen A.\u2005B. de Oliveira G.\u2005R. Pereira \u2018Antimalarial naphthoquinones. Synthesis via click chemistry in\u2005vitro activity docking to PfDHODH and SAR of lapachol-based compounds\u2019 Eur. J. Med. Chem.2018 145 191\u2013205.","DOI":"10.1016\/j.ejmech.2017.12.051"},{"key":"e_1_2_7_32_1","doi-asserted-by":"crossref","unstructured":"E.-J. Lee H.-J. Lee H.\u2005J. Park H.-Y. Min M.-E. Suh H.-J. Chung S.\u2005K. Lee \u2018Induction of G2\/M cell cycle arrest and apoptosis by a benz[f]indole-4 9-dione analog in cultured human lung (A549) cancer cells\u2019 Bioorg. Med. Chem. Lett.2004 14 5175\u20135178.","DOI":"10.1016\/j.bmcl.2004.07.062"},{"key":"e_1_2_7_33_1","doi-asserted-by":"crossref","unstructured":"G.-Y. Song Y. Kim X.-G. Zheng Y.-J. You H. Cho J.-H. Chung D.-E. Sok B.-Z. Ahn \u2018Naphthazarin derivatives (IV): synthesis inhibition of DNA topoisomerase I and cytotoxicity of 2- or 6-acyl-5 8-dimethoxy-1 4-naphthoquinones\u2019 Eur. J. Med. Chem.2000 35 291\u2013298.","DOI":"10.1016\/S0223-5234(00)00129-X"},{"key":"e_1_2_7_34_1","doi-asserted-by":"crossref","unstructured":"A.\u2005E. Shchekotikhin V.\u2005N. Buyanov M.\u2005N. Preobrazhenskaya \u2018Synthesis of 1-(\u03c9-aminoalkyl) naphthoindolediones with antiproliferative properties\u2019 Bioorg. Med. Chem.2004 12 3923\u20133930.","DOI":"10.1016\/j.bmc.2004.04.042"},{"key":"e_1_2_7_35_1","doi-asserted-by":"crossref","unstructured":"T. Tran E. Saheba A.\u2005V. Arcerio V. Chavez Q.-Y. Li L.\u2005E. Martinez T.\u2005P. Primm \u2018Quinones as antimycobacterial agents\u2019 Bioorg. Med. Chem.2004 12 4809\u20134813.","DOI":"10.1016\/j.bmc.2004.07.015"},{"key":"e_1_2_7_36_1","doi-asserted-by":"crossref","unstructured":"J.-C. Lien L.-J. Huang J.-P. Wang C.-M. Teng K.-H. Lee S.-C. Kuo \u2018Synthesis and antiplatelet anti-inflammatory and antiallergic activities of 2-substituted 3-chloro-1 4-naphthoquinone derivatives\u2019 Bioorg. Med. Chem.1997 5 2111\u20132120.","DOI":"10.1016\/S0968-0896(97)00133-8"},{"key":"e_1_2_7_37_1","doi-asserted-by":"crossref","unstructured":"E.\u2005V.\u2005M. dos Santos J.\u2005W.\u2005D.\u2005M. Carneiro V.\u2005F. Ferreira \u2018Quantitative structure\u2013activity relationship in aziridinyl-1 4-naphthoquinone antimalarials: study of theoretical correlations by the PM3 method\u2019 Bioorg. Med. Chem.2004 12 87\u201393.","DOI":"10.1016\/j.bmc.2003.10.022"},{"key":"e_1_2_7_38_1","doi-asserted-by":"crossref","unstructured":"J.\u2005A. Valderrama J. Benites M. Cortes H. Pessoa-Mahana E. Prina A. Fournet \u2018Studies on quinones. Part\u200538: Synthesis and leishmanicidal activity of sesquiterpene 1 4-quinones\u2019 Bioorg. Med. Chem.2003 11 4713\u20134718.","DOI":"10.1016\/j.bmc.2003.08.011"},{"key":"e_1_2_7_39_1","doi-asserted-by":"crossref","unstructured":"A. Ouahrouch H. Ighachane M. Taourirte J.\u2005W. Engels M.\u2005H. Sedra H.\u2005B. Lazrek \u2018Benzimidazole-1 2 3-triazole Hybrid Molecules: Synthesis and Evaluation for Antibacterial\/Antifungal Activity\u2019 Arch. Pharm.2014 347 748\u2013755.","DOI":"10.1002\/ardp.201400142"},{"key":"e_1_2_7_40_1","doi-asserted-by":"crossref","unstructured":"F. Pisaneschi Q.-D. Nguyen Shamsaei E. Glaser E. Robins M. Kaliszczak G. Smith A.\u2005C. Spivey E.\u2005O. Aboagye \u2018Development of a new epidermal growth factor receptor positron emission tomography imaging agent based on the 3-cyanoquinoline core: Synthesis and biological evaluation\u2019 Bioorg. Med. Chem.2010 18 6634\u20136645.","DOI":"10.1016\/j.bmc.2010.08.004"},{"key":"e_1_2_7_41_1","doi-asserted-by":"crossref","unstructured":"V. Sumangala B. Poojary N. Chidananda J. Fernandes N.\u2005S. Kumari \u2018Synthesis and antimicrobial activity of 1 2 3-triazoles containing quinoline moiety\u2019 Arch. Pharmacal Res.2010 33 1911\u20131918.","DOI":"10.1007\/s12272-010-1204-3"},{"key":"e_1_2_7_42_1","doi-asserted-by":"crossref","unstructured":"L.\u2005B. Peterson B.\u2005S. Blagg \u2018Click chemistry to probe Hsp90: synthesis and evaluation of a series of triazole-containing novobiocin analogues\u2019 Bioorg. Med. Chem. Lett.2010 20 3957\u20133960.","DOI":"10.1016\/j.bmcl.2010.04.140"},{"key":"e_1_2_7_43_1","doi-asserted-by":"crossref","unstructured":"C. Le Manach A. Baron R. Guillot B. Vauzeilles J.-M. Beau \u2018Design and synthesis by click triazole formation of paclitaxel mimics with simplified core and side-chain structures\u2019 Tetrahedron Lett.2011 52 1462\u20131465.","DOI":"10.1016\/j.tetlet.2011.01.081"},{"key":"e_1_2_7_44_1","doi-asserted-by":"crossref","unstructured":"T.\u2005O. Olomola R. Klein K.\u2005A. Lobb Y. Sayed P.\u2005T. Kaye \u2018Towards the synthesis of coumarin derivatives as potential dual-action HIV-1 protease and reverse transcriptase inhibitors\u2019 Tetrahedron Lett.2010 51 6325\u20136328.","DOI":"10.1016\/j.tetlet.2010.09.121"},{"key":"e_1_2_7_45_1","doi-asserted-by":"crossref","unstructured":"A. Keivanloo M. Bakherad M. Lotfi \u2018Use of ligand-assisted click reactions for the rapid synthesis of novel 1 2 3-triazole pharmacophore-based 1 2 4-triazines and their benzo-fused analogues\u2019 Tetrahedron2017 73 5872\u20135882.","DOI":"10.1016\/j.tet.2017.08.041"},{"key":"e_1_2_7_46_1","doi-asserted-by":"crossref","unstructured":"C. Ornelas J. Ruiz Aranzaes E. Cloutet S. Alves D. Astruc \u2018Click assembly of 1 2 3-triazole-linked dendrimers including ferrocenyl dendrimers which sense both oxo anions and metal cations\u2019 Angew. Chem.2007 119 890\u2013895.","DOI":"10.1002\/ange.200602858"},{"key":"e_1_2_7_47_1","doi-asserted-by":"crossref","unstructured":"J.\u2005M. Andrews \u2018Determination of minimum inhibitory concentrations\u2019 J. Antimicrob. Chemother.2001 48 5\u201316.","DOI":"10.1093\/jac\/48.suppl_1.5"},{"key":"e_1_2_7_48_1","doi-asserted-by":"crossref","unstructured":"M.\u2005T. Yilmaz \u2018Minimum inhibitory and minimum bactericidal concentrations of boron compounds against several bacterial strains\u2019 Turk. J. Med. Sci.2012 42 1423\u20131429.","DOI":"10.3906\/sag-1205-83"},{"key":"e_1_2_7_49_1","doi-asserted-by":"crossref","unstructured":"N.\u2005O. Mahmoodi J. Parvizi B. Sharifzadeh M. Rassa \u2018Facile Regioselective Synthesis of Novel bis-Thiazole Derivatives and Their Antimicrobial Activity\u2019 Arch. Pharm.2013 346 860\u2013864.","DOI":"10.1002\/ardp.201300187"},{"key":"e_1_2_7_50_1","doi-asserted-by":"crossref","unstructured":"M. Vaara \u2018Agents that increase the permeability of the outer membrane\u2019 Microbiol. Rev.1992 56 395\u2013411.","DOI":"10.1128\/mr.56.3.395-411.1992"},{"key":"e_1_2_7_51_1","doi-asserted-by":"crossref","unstructured":"M. Sim\u00f5es S. Rocha M.\u2005A. Coimbra M.\u2005J. Vieira \u2018Enhancement ofEscherichia coliandStaphylococcus aureusantibiotic susceptibility using sesquiterpenoids\u2019 Med. Chem.2008 4 616\u2013623.","DOI":"10.2174\/157340608786242016"},{"key":"e_1_2_7_52_1","doi-asserted-by":"crossref","unstructured":"S. Sepehri S. Soleymani R. Zabihollahi M.\u2005R. Aghasadeghi M. Sadat L. Saghaie A. Fassihi \u2018Synthesis Biological Evaluation and Molecular Docking Studies of Novel 4-[4-Arylpyridin-1(4H)-yl]benzoic Acid Derivatives as Anti-HIV-1 Agents\u2019 Chem. Biodiversity2017 14 e1700295.","DOI":"10.1002\/cbdv.201700295"},{"key":"e_1_2_7_53_1","doi-asserted-by":"crossref","unstructured":"N. Fani A. Bordbar Y. Ghayeb S. Sepehri \u2018Computational design of Tryprostatin-A derivatives as novel \u03b1\u03b2-tubulin inhibitors\u2019 J. Biomol. Struct. Dyn.2015 33 471\u2013486.","DOI":"10.1080\/07391102.2014.892028"}],"container-title":["Chemistry &amp; Biodiversity"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1002%2Fcbdv.201800410","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/cbdv.201800410","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/full-xml\/10.1002\/cbdv.201800410","content-type":"application\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/cbdv.201800410","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,9,14]],"date-time":"2023-09-14T07:19:06Z","timestamp":1694675946000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/cbdv.201800410"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2018,12,13]]},"references-count":53,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2019,1]]}},"alternative-id":["10.1002\/cbdv.201800410"],"URL":"https:\/\/doi.org\/10.1002\/cbdv.201800410","archive":["Portico"],"relation":{},"ISSN":["1612-1872","1612-1880"],"issn-type":[{"value":"1612-1872","type":"print"},{"value":"1612-1880","type":"electronic"}],"subject":[],"published":{"date-parts":[[2018,12,13]]},"assertion":[{"value":"2018-08-14","order":0,"name":"received","label":"Received","group":{"name":"publication_history","label":"Publication History"}},{"value":"2018-10-18","order":1,"name":"accepted","label":"Accepted","group":{"name":"publication_history","label":"Publication History"}},{"value":"2018-12-13","order":2,"name":"published","label":"Published","group":{"name":"publication_history","label":"Publication History"}}],"article-number":"e1800410"}}