1 Ocak 1996 Dergi makalesi Açık Erişim

Topcu, G; Ulubelen, A; Tam, TCM; Che, CT

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  <identifier identifierType="URL">https://aperta.ulakbim.gov.tr/record/101355</identifier>
  <creators>
    <creator>
      <creatorName>Topcu, G</creatorName>
      <givenName>G</givenName>
      <familyName>Topcu</familyName>
    </creator>
    <creator>
      <creatorName>Ulubelen, A</creatorName>
      <givenName>A</givenName>
      <familyName>Ulubelen</familyName>
    </creator>
    <creator>
      <creatorName>Tam, TCM</creatorName>
      <givenName>TCM</givenName>
      <familyName>Tam</familyName>
    </creator>
    <creator>
      <creatorName>Che, CT</creatorName>
      <givenName>CT</givenName>
      <familyName>Che</familyName>
    </creator>
  </creators>
  <titles>
    <title>Norditerpenes And Norsesterterpenes From Salvia Yosgadensis</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/101355</alternateIdentifier>
  </alternateIdentifiers>
  <relatedIdentifiers>
    <relatedIdentifier relatedIdentifierType="DOI" relationType="IsVersionOf">10.81043/aperta.101354</relatedIdentifier>
    <relatedIdentifier relatedIdentifierType="DOI" relationType="IsIdenticalTo">10.81043/aperta.101355</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">The aerial parts of Salvia yosgadensis afforded five new terpenes with unusual skeletons, together with two known norditerpenes, ambreinolide and norambreinolide. The new compounds were elucidated as 6 alpha-hydroxyambreinolide, 6 alpha-hydroxynorambreinolide, 6 alpha-hydroxy-8 alpha-acetoxy-13,14,15,16-tetranorlabdan-12-oic acid, and two 19,20-dinorsesterterpenes, named as yosgadensonol and 13-epi-yosgadensonol. Their structures were determined by spectroscopic means, particularly by extensive 1D and 2D NMR studies.</description>
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