1 Ocak 1995 Dergi makalesi Açık Erişim

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

Dublin Core

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  <dc:creator>ULUBELEN, A</dc:creator>
  <dc:creator>GOREN, N</dc:creator>
  <dc:creator>JIANG, TY</dc:creator>
  <dc:creator>SCOTT, L</dc:creator>
  <dc:creator>TIANASOARAMOMOJY, M</dc:creator>
  <dc:creator>SNYDER, JK</dc:creator>
  <dc:date>1995-01-01</dc:date>
  <dc:description>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.</dc:description>
  <dc:identifier>https://aperta.ulakbim.gov.trrecord/102601</dc:identifier>
  <dc:identifier>oai:zenodo.org:102601</dc:identifier>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>http://www.opendefinition.org/licenses/cc-by</dc:rights>
  <dc:source>MAGNETIC RESONANCE IN CHEMISTRY 33(11) 900-904</dc:source>
  <dc:title>NMR ASSIGNMENTS AND ABSOLUTE STEREOCHEMISTRY OF 2 GUAIANOLIDE SESQUITERPENES FROM TANACETUM-DENSUM SUBSP AMANI</dc:title>
  <dc:type>info:eu-repo/semantics/article</dc:type>
  <dc:type>publication-article</dc:type>
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