1,2-Diborolanes With Strong Donor Substituents: Synthesis and High Antimicrobial Activity
| dc.contributor.author | Şahin, Yüksel | |
| dc.contributor.author | Poyrazoğlu Çoban, Esin | |
| dc.contributor.author | Sevinçek, Resul | |
| dc.contributor.author | Bıyık, Halil H. | |
| dc.contributor.author | Özgener, Hüseyin | |
| dc.contributor.author | Aygün, Muhittin | |
| dc.coverage.doi | 10.1016/j.bioorg.2020.104494 | |
| dc.date.accessioned | 2021-01-24T18:33:09Z | |
| dc.date.available | 2021-01-24T18:33:09Z | |
| dc.date.issued | 2021 | |
| dc.description.abstract | 1,2-diborolanes with strong and without strong donor substituents have been described, and are also referred to as 1,2-diboracyclopentane. The 1,2-diaryl/alkyl-amino-1,2-diboracyclopentanes 2, 3, and 4 were obtained in good yield after the reaction of 1,2-dichloro-1,2-diboracyclopentane 1 with ArNHLi and Me3Si-NR2. The structures of these new derivatives were characterized by nuclear magnetic resonance spectroscopy. The molecular structures of 2b, 2c, 2e, 4, and 5f were also determined by single-crystal X-ray diffraction. The newly synthesized 1,2-borolanes are stable in air and showed particularly high activity against some Gram-positive bacteria. © 2020 Elsevier Inc. | en_US |
| dc.description.sponsorship | This study was supported by Adnan Menderes University BAP (project No: FEF-20011 and FEF-17004). The authors also acknowledge Dokuz Eylül University for the use of the Agilent Xcalibur Eos diffractometer (purchased under University Research Grant no.2010.KB.FEN.13). | en_US |
| dc.identifier.doi | 10.1016/j.bioorg.2020.104494 | |
| dc.identifier.issn | 0045-2068 | |
| dc.identifier.issn | 1090-2120 | |
| dc.identifier.scopus | 2-s2.0-85097038853 | |
| dc.identifier.uri | https://doi.org/10.1016/j.bioorg.2020.104494 | |
| dc.identifier.uri | https://hdl.handle.net/11147/10233 | |
| dc.language.iso | en | en_US |
| dc.publisher | Academic Press | en_US |
| dc.relation.ispartof | Bioorganic Chemistry | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.subject | Antimicrobial | en_US |
| dc.subject | Diboracyclopentane | en_US |
| dc.subject | Diborolane | en_US |
| dc.subject | Heterocycles | en_US |
| dc.title | 1,2-Diborolanes With Strong Donor Substituents: Synthesis and High Antimicrobial Activity | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication | |
| gdc.author.institutional | Özgener, Hüseyin | |
| gdc.bip.impulseclass | C4 | |
| gdc.bip.influenceclass | C5 | |
| gdc.bip.popularityclass | C4 | |
| gdc.coar.access | metadata only access | |
| gdc.coar.type | text::journal::journal article | |
| gdc.collaboration.industrial | false | |
| gdc.description.department | İzmir Institute of Technology. Chemistry | en_US |
| gdc.description.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
| gdc.description.scopusquality | Q2 | |
| gdc.description.volume | 106 | |
| gdc.description.wosquality | Q1 | |
| gdc.identifier.openalex | W3106242366 | |
| gdc.identifier.pmid | 33268009 | |
| gdc.identifier.wos | WOS:000605008800001 | |
| gdc.index.type | WoS | |
| gdc.index.type | Scopus | |
| gdc.index.type | PubMed | |
| gdc.oaire.accesstype | HYBRID | |
| gdc.oaire.diamondjournal | false | |
| gdc.oaire.impulse | 7.0 | |
| gdc.oaire.influence | 3.0323897E-9 | |
| gdc.oaire.isgreen | false | |
| gdc.oaire.keywords | Boron Compounds | |
| gdc.oaire.keywords | Structure-Activity Relationship | |
| gdc.oaire.keywords | Dose-Response Relationship, Drug | |
| gdc.oaire.keywords | Molecular Structure | |
| gdc.oaire.keywords | Microbial Sensitivity Tests | |
| gdc.oaire.keywords | Gram-Positive Bacteria | |
| gdc.oaire.keywords | Anti-Bacterial Agents | |
| gdc.oaire.popularity | 8.5523E-9 | |
| gdc.oaire.publicfunded | false | |
| gdc.oaire.sciencefields | 01 natural sciences | |
| gdc.oaire.sciencefields | 0104 chemical sciences | |
| gdc.openalex.collaboration | National | |
| gdc.openalex.fwci | 0.63509355 | |
| gdc.openalex.normalizedpercentile | 0.6 | |
| gdc.opencitations.count | 8 | |
| gdc.plumx.crossrefcites | 8 | |
| gdc.plumx.mendeley | 4 | |
| gdc.plumx.scopuscites | 9 | |
| gdc.scopus.citedcount | 9 | |
| gdc.wos.citedcount | 8 | |
| relation.isAuthorOfPublication.latestForDiscovery | 217feea8-1199-49fc-9e0b-db147778bc4d | |
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