Dergi makalesi Açık Erişim
ULUBELEN, A; GOREN, N; JIANG, TY; SCOTT, L; TIANASOARAMOMOJY, M; SNYDER, JK
{ "@context": "https://schema.org/", "@id": 102601, "@type": "ScholarlyArticle", "creator": [ { "@type": "Person", "name": "ULUBELEN, A" }, { "@type": "Person", "name": "GOREN, N" }, { "@type": "Person", "name": "JIANG, TY" }, { "@type": "Person", "name": "SCOTT, L" }, { "@type": "Person", "name": "TIANASOARAMOMOJY, M" }, { "@type": "Person", "name": "SNYDER, JK" } ], "datePublished": "1995-01-01", "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.", "headline": "NMR ASSIGNMENTS AND ABSOLUTE STEREOCHEMISTRY OF 2 GUAIANOLIDE SESQUITERPENES FROM TANACETUM-DENSUM SUBSP AMANI", "identifier": 102601, "image": "https://aperta.ulakbim.gov.tr/static/img/logo/aperta_logo_with_icon.svg", "license": "http://www.opendefinition.org/licenses/cc-by", "name": "NMR ASSIGNMENTS AND ABSOLUTE STEREOCHEMISTRY OF 2 GUAIANOLIDE SESQUITERPENES FROM TANACETUM-DENSUM SUBSP AMANI", "url": "https://aperta.ulakbim.gov.tr/record/102601" }
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