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
relation.isOrgUnitOfPublication.latestForDiscovery 9af2b05f-28ac-4011-8abe-a4dfe192da5e

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