Dergi makalesi Açık Erişim
Kaya, Afsin Ahmet; Sengul, Mehmet Emin; Menzek, Abdullah; Kayaardi, Ibrahim; Karakus, Murat; Sahin, Ertan
{ "@context": "https://schema.org/", "@id": 21371, "@type": "ScholarlyArticle", "creator": [ { "@type": "Person", "name": "Kaya, Afsin Ahmet" }, { "@type": "Person", "affiliation": "Ataturk Univ, Dept Chem, Fac Sci, TR-25240 Erzurum, Turkey", "name": "Sengul, Mehmet Emin" }, { "@type": "Person", "affiliation": "Ataturk Univ, Dept Chem, Fac Sci, TR-25240 Erzurum, Turkey", "name": "Menzek, Abdullah" }, { "@type": "Person", "affiliation": "Ataturk Univ, Dept Chem, Fac Sci, TR-25240 Erzurum, Turkey", "name": "Kayaardi, Ibrahim" }, { "@type": "Person", "affiliation": "Ataturk Univ, Dept Chem, Fac Sci, TR-25240 Erzurum, Turkey", "name": "Karakus, Murat" }, { "@type": "Person", "affiliation": "Ataturk Univ, Dept Chem, Fac Sci, TR-25240 Erzurum, Turkey", "name": "Sahin, Ertan" } ], "datePublished": "2011-01-01", "description": "Each adduct of alpha-terpinene with p-quinone and 1,4-naphthoquinone in Ac(2)O/Et(3)N at 180 C gives two aromatic products, one of which had a distinctive smell formed by the loss of an ethylene group. Here, we report the crystal structure of (1RS, 4RS)-1-isopropyl-4-methyl-1,4-dihydro-1,4-ethanoanthracene-9,10-diyl diacetate. It is crystallised in an orthorhombic space group, Pbca, with cell dimensions a = 10.2899(7), b = 19.7804(9), c = 19.7519(8) angstrom and Z = 8. According to its NMR and X-ray diffraction data, the isopropyl and acetate groups slowly rotate.", "headline": "Aromatisation in adducts of alpha-terpinene: Influence of hindered internal rotations", "identifier": 21371, "image": "https://aperta.ulakbim.gov.tr/static/img/logo/aperta_logo_with_icon.svg", "license": "http://www.opendefinition.org/licenses/cc-by", "name": "Aromatisation in adducts of alpha-terpinene: Influence of hindered internal rotations", "url": "https://aperta.ulakbim.gov.tr/record/21371" }
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