1 Ocak 1995 Dergi makalesi Açık Erişim

ULUBELEN, A; GOREN, N; JIANG, TY; SCOTT, L; TIANASOARAMOMOJY, M; SNYDER, JK

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  <identifier identifierType="URL">https://aperta.ulakbim.gov.tr/record/102601</identifier>
  <creators>
    <creator>
      <creatorName>ULUBELEN, A</creatorName>
      <givenName>A</givenName>
      <familyName>ULUBELEN</familyName>
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    <creator>
      <creatorName>GOREN, N</creatorName>
      <givenName>N</givenName>
      <familyName>GOREN</familyName>
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    <creator>
      <creatorName>JIANG, TY</creatorName>
      <givenName>TY</givenName>
      <familyName>JIANG</familyName>
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    <creator>
      <creatorName>SCOTT, L</creatorName>
      <givenName>L</givenName>
      <familyName>SCOTT</familyName>
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    <creator>
      <creatorName>TIANASOARAMOMOJY, M</creatorName>
      <givenName>M</givenName>
      <familyName>TIANASOARAMOMOJY</familyName>
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    <creator>
      <creatorName>SNYDER, JK</creatorName>
      <givenName>JK</givenName>
      <familyName>SNYDER</familyName>
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  <titles>
    <title>Nmr Assignments And Absolute Stereochemistry Of 2 Guaianolide Sesquiterpenes From Tanacetum-Densum Subsp Amani</title>
  </titles>
  <publisher>Aperta</publisher>
  <publicationYear>1995</publicationYear>
  <dates>
    <date dateType="Issued">1995-01-01</date>
  </dates>
  <resourceType resourceTypeGeneral="Text">Journal article</resourceType>
  <alternateIdentifiers>
    <alternateIdentifier alternateIdentifierType="url">https://aperta.ulakbim.gov.tr/record/102601</alternateIdentifier>
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    <relatedIdentifier relatedIdentifierType="DOI" relationType="IsVersionOf">10.81043/aperta.102600</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 guaianolide sesquiterpene pyrethroidinin (1) and the corresponding ketone parishin A (2) were isolated from Tanacetum densum subsp, amani (Asteraceae). The absolute stereochemistry of 1 was established as (1R, 3R, 6S, 7S, 10R) on the basis of the differential shielding in the H-1 NMR spectra of the (-)- and (+)-O-methylmandelate esters. The structure, including absolute stereochemistry, of 2 was confirmed by oxidation of 1 with Jones' reagent.</description>
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