Dergi makalesi Açık Erişim
ULUBELEN, A; MERICLI, AH; MERICLI, F; KAYA, U
<?xml version='1.0' encoding='utf-8'?> <resource xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns="http://datacite.org/schema/kernel-4" xsi:schemaLocation="http://datacite.org/schema/kernel-4 http://schema.datacite.org/meta/kernel-4.1/metadata.xsd"> <identifier identifierType="URL">https://aperta.ulakbim.gov.tr/record/102085</identifier> <creators> <creator> <creatorName>ULUBELEN, A</creatorName> <givenName>A</givenName> <familyName>ULUBELEN</familyName> </creator> <creator> <creatorName>MERICLI, AH</creatorName> <givenName>AH</givenName> <familyName>MERICLI</familyName> </creator> <creator> <creatorName>MERICLI, F</creatorName> <givenName>F</givenName> <familyName>MERICLI</familyName> </creator> <creator> <creatorName>KAYA, U</creatorName> <givenName>U</givenName> <familyName>KAYA</familyName> </creator> </creators> <titles> <title>An Alkaloid And Lignans From Haplophyllum Telepnioides</title> </titles> <publisher>Aperta</publisher> <publicationYear>1994</publicationYear> <dates> <date dateType="Issued">1994-01-01</date> </dates> <resourceType resourceTypeGeneral="Text">Journal article</resourceType> <alternateIdentifiers> <alternateIdentifier alternateIdentifierType="url">https://aperta.ulakbim.gov.tr/record/102085</alternateIdentifier> </alternateIdentifiers> <relatedIdentifiers> <relatedIdentifier relatedIdentifierType="DOI" relationType="IsVersionOf">10.81043/aperta.102084</relatedIdentifier> <relatedIdentifier relatedIdentifierType="DOI" relationType="IsIdenticalTo">10.81043/aperta.102085</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">Haplophyllum telephioides yielded a new alkaloid, 7-hydroxy-9-methoxyflindersine and a new lignan 4-acetyldiphyllin, in addition to haplomyrtin, diphyllin and vanillic acid. The structures were established from spectral data.</description> </descriptions> </resource>
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