1 Ocak 2012 Dergi makalesi Açık Erişim

Kahriman, Nuran; Iskender, Nagihan Yilmaz; Yucel, Murat; Yayli, Nurettin; Demir, Emine; Demirbag, Zihni

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  <identifier identifierType="URL">https://aperta.ulakbim.gov.tr/record/84883</identifier>
  <creators>
    <creator>
      <creatorName>Kahriman, Nuran</creatorName>
      <givenName>Nuran</givenName>
      <familyName>Kahriman</familyName>
      <affiliation>Karadeniz Tech Univ, Fac Sci, Dept Chem, TR-61080 Trabzon, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Iskender, Nagihan Yilmaz</creatorName>
      <givenName>Nagihan Yilmaz</givenName>
      <familyName>Iskender</familyName>
      <affiliation>Karadeniz Tech Univ, Fac Sci, Dept Chem, TR-61080 Trabzon, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Yucel, Murat</creatorName>
      <givenName>Murat</givenName>
      <familyName>Yucel</familyName>
      <affiliation>Karadeniz Tech Univ, Fac Sci, Dept Chem, TR-61080 Trabzon, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Yayli, Nurettin</creatorName>
      <givenName>Nurettin</givenName>
      <familyName>Yayli</familyName>
      <affiliation>Karadeniz Tech Univ, Fac Sci, Dept Chem, TR-61080 Trabzon, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Demir, Emine</creatorName>
      <givenName>Emine</givenName>
      <familyName>Demir</familyName>
      <affiliation>Karadeniz Tech Univ, Fac Sci, Dept Biol, TR-61080 Trabzon, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Demirbag, Zihni</creatorName>
      <givenName>Zihni</givenName>
      <familyName>Demirbag</familyName>
      <affiliation>Karadeniz Tech Univ, Fac Sci, Dept Biol, TR-61080 Trabzon, Turkey</affiliation>
    </creator>
  </creators>
  <titles>
    <title>Microwave-Assisted Synthesis Of 1,3 '-Diaza-Flavanone/Flavone And Their Alkyl Derivatives With Antimicrobial Activity</title>
  </titles>
  <publisher>Aperta</publisher>
  <publicationYear>2012</publicationYear>
  <dates>
    <date dateType="Issued">2012-01-01</date>
  </dates>
  <resourceType resourceTypeGeneral="Text">Journal article</resourceType>
  <alternateIdentifiers>
    <alternateIdentifier alternateIdentifierType="url">https://aperta.ulakbim.gov.tr/record/84883</alternateIdentifier>
  </alternateIdentifiers>
  <relatedIdentifiers>
    <relatedIdentifier relatedIdentifierType="DOI" relationType="IsIdenticalTo">10.1002/jhet.800</relatedIdentifier>
  </relatedIdentifiers>
  <rightsList>
    <rights rightsURI="http://www.opendefinition.org/licenses/cc-by">Creative Commons Attribution</rights>
    <rights rightsURI="info:eu-repo/semantics/openAccess">Open Access</rights>
  </rightsList>
  <descriptions>
    <description descriptionType="Abstract">A simple environmentally friendly solid-phase microwave-assisted method was used to synthesis of the 1,3'-diazaflavanone (2) and 1,3'-diazaflavone (3) from the cyclization of 2'-amino (E)-3?-azachalcone (1). Ten new N-alkyl (C512,14,15)-substituted 1,3'-diazaflavanonium bromides (2aj) were prepared from compound 2 with corresponding alkyl halides in acetonitrile under reflux. In addition, nine new N,N'-dialkyl (C512,14)-substituted 1,3'-diazaflavonium bromides (3ai) were also synthesized from compound 3 with corresponding alkyl halides using basic silica in acetonitrile. The antimicrobial activities of compounds 13, 2aj, and 3ai were tested against Gram-positive (G+) (Bacillus subtilis, Staphylococcus epidermidis, Staphylococcus aureus, and Enterococcus faecalis) and Gram-negative (G-) (Escherichia coli, Klebsiella pneumonia, Pseudomonas aeruginosa, Proteus vulgaris, Salmonella typhimirium, Yersinia pseudotuberculosis, and Enterobacter cloaceae) microorganisms. They showed good antimicrobial activity against the Gram-positive bacteria tested with the minimal inhibitory concentration values less than 7.8 mu g/mL in most cases. The optimum length of the alkyl chain for better and broader activity is situated in the range of 912 carbon atoms in the series of compounds 2aj and five to six carbon atoms in the series of compounds 3ai. The nonalkylated compounds 13 were not effective, as were the ones alkylated with five or six C alkyl groups (2a and 2b) and 813 C alkyl groups for N,N'-dialkyl compounds (3c3i). The antimicrobial activity increased as the length of the alkyl substitution increased from 8 to 12 carbons in compounds 2aj. However, antimicrobial activity decreased as the length of the alkyl substitution increased from 7 to 13 carbons in compounds 3ci. J. Heterocyclic Chem., (2012)</description>
  </descriptions>
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