1 Ocak 1996 Dergi makalesi Açık Erişim

Topcu, G; Eris, C; Kurucu, S; Ulubelen, A

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  <identifier identifierType="URL">https://aperta.ulakbim.gov.tr/record/102211</identifier>
  <creators>
    <creator>
      <creatorName>Topcu, G</creatorName>
      <givenName>G</givenName>
      <familyName>Topcu</familyName>
    </creator>
    <creator>
      <creatorName>Eris, C</creatorName>
      <givenName>C</givenName>
      <familyName>Eris</familyName>
    </creator>
    <creator>
      <creatorName>Kurucu, S</creatorName>
      <givenName>S</givenName>
      <familyName>Kurucu</familyName>
    </creator>
    <creator>
      <creatorName>Ulubelen, A</creatorName>
      <givenName>A</givenName>
      <familyName>Ulubelen</familyName>
    </creator>
  </creators>
  <titles>
    <title>A New Flavanone From Teucrium Alyssifolium</title>
  </titles>
  <publisher>Aperta</publisher>
  <publicationYear>1996</publicationYear>
  <dates>
    <date dateType="Issued">1996-01-01</date>
  </dates>
  <resourceType resourceTypeGeneral="Text">Journal article</resourceType>
  <alternateIdentifiers>
    <alternateIdentifier alternateIdentifierType="url">https://aperta.ulakbim.gov.tr/record/102211</alternateIdentifier>
  </alternateIdentifiers>
  <relatedIdentifiers>
    <relatedIdentifier relatedIdentifierType="DOI" relationType="IsVersionOf">10.81043/aperta.102210</relatedIdentifier>
    <relatedIdentifier relatedIdentifierType="DOI" relationType="IsIdenticalTo">10.81043/aperta.102211</relatedIdentifier>
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  <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">From the aerial parts of Teucrium alyssifolium in addition to previously obtained neo-clerodane diterpenoids, a new flavanone alysifolinone and three flavones cirsiliol, cirsilineol and luteolin-6, 7, 3', 4'-tetramethyl ether, were isolated. The structure of the compounds was established by spectral data, and by TLC comparison for the known compounds.</description>
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