{"@context":{"@vocab":"https://cir.nii.ac.jp/schema/1.0/","rdfs":"http://www.w3.org/2000/01/rdf-schema#","dc":"http://purl.org/dc/elements/1.1/","dcterms":"http://purl.org/dc/terms/","foaf":"http://xmlns.com/foaf/0.1/","prism":"http://prismstandard.org/namespaces/basic/2.0/","cinii":"http://ci.nii.ac.jp/ns/1.0/","datacite":"https://schema.datacite.org/meta/kernel-4/","ndl":"http://ndl.go.jp/dcndl/terms/","jpcoar":"https://github.com/JPCOAR/schema/blob/master/2.0/"},"@id":"https://cir.nii.ac.jp/crid/1360002219111150720.json","@type":"Article","productIdentifier":[{"identifier":{"@type":"DOI","@value":"10.1246/cl.2008.50"}},{"identifier":{"@type":"URI","@value":"https://academic.oup.com/chemlett/article-pdf/37/1/50/55596999/cl.2008.50.pdf"}},{"identifier":{"@type":"DOI","@value":"10.1002/chin.200824102"}},{"identifier":{"@type":"NAID","@value":"10020147756"}}],"dc:title":[{"@value":"One-step Synthesis of Dibutyl Furandicarboxylates from Galactaric Acid"}],"description":[{"type":"abstract","notation":[{"@value":"<jats:title>Abstract</jats:title>\n               <jats:p>Dibutyl 2,5-furandicarboxylate (2) and dibutyl 2,3-furandicarboxylate (3) were synthesized using one step from galactaric acid and 1-butanol. Sulfuric acid, p-toluenesulfonic acid, and heteropolyacids were good catalysts for the reaction. The reaction time was dependent on the amount of the catalyst, but the final yields of the main product, 2 remained unchanged.</jats:p>"}]}],"creator":[{"@id":"https://cir.nii.ac.jp/crid/1580572701018582016","@type":"Researcher","personIdentifier":[{"@type":"NRID","@value":"9000000079701"}],"foaf:name":[{"@value":"Yoichi Taguchi"}],"jpcoar:affiliationName":[{"@value":"National Institute of Advanced Industrial Science and Technology (AIST)"}]},{"@id":"https://cir.nii.ac.jp/crid/1580572701018582018","@type":"Researcher","personIdentifier":[{"@type":"NRID","@value":"9000005151403"}],"foaf:name":[{"@value":"Akihiro Oishi"}],"jpcoar:affiliationName":[{"@value":"National Institute of Advanced Industrial Science and Technology (AIST)"}]},{"@id":"https://cir.nii.ac.jp/crid/1580572701018582017","@type":"Researcher","personIdentifier":[{"@type":"NRID","@value":"9000002048317"}],"foaf:name":[{"@value":"Hiroshi Iida"}],"jpcoar:affiliationName":[{"@value":"National Institute of Advanced Industrial Science and Technology (AIST)"}]}],"publication":{"publicationIdentifier":[{"@type":"PISSN","@value":"03667022"},{"@type":"EISSN","@value":"13480715"},{"@type":"PISSN","@value":"09317597"},{"@type":"EISSN","@value":"15222667"},{"@type":"NCID","@value":"AA00603318"}],"prism:publicationName":[{"@value":"Chemistry Letters"}],"dc:publisher":[{"@value":"Oxford University Press (OUP)"}],"prism:publicationDate":"2007-12-01","prism:volume":"37","prism:number":"1","prism:startingPage":"50","prism:endingPage":"51"},"reviewed":"false","dc:rights":["https://academic.oup.com/pages/standard-publication-reuse-rights"],"url":[{"@id":"https://academic.oup.com/chemlett/article-pdf/37/1/50/55596999/cl.2008.50.pdf"}],"createdAt":"2007-12-03","modifiedAt":"2024-01-18","relatedProduct":[{"@id":"https://cir.nii.ac.jp/crid/1360285705084641408","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Enzymes Suitable for Biorefinery to Coproduce Hexaric Acids and Electricity from Hexuronic Acids Derived from Biomass"}]},{"@id":"https://cir.nii.ac.jp/crid/1360848657305665792","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Pyrroloquinoline quinone-dependent glucose dehydrogenase anode: d-Galacturonic acid oxidation and galactaric acid production"}]},{"@id":"https://cir.nii.ac.jp/crid/1361418520982380288","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Oxydation catalytique du HMF en acide 2,5-furane dicarboxylique"}]},{"@id":"https://cir.nii.ac.jp/crid/1361699995042657280","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"A new approach for the production of 2,5-furandicarboxylic acid by in situ oxidation of 5-hydroxymethylfurfural starting from fructose"}]},{"@id":"https://cir.nii.ac.jp/crid/1361981468485219840","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Polyesters Derived from Furan and Tetrahydrofuran Nuclei"}]},{"@id":"https://cir.nii.ac.jp/crid/1362544421417109120","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Cooperative effect of cobalt acetylacetonate and silica in the catalytic cyclization and oxidation of fructose to 2,5-furandicarboxylic acid"}]},{"@id":"https://cir.nii.ac.jp/crid/1370299146793288704","@type":"Product","relationType":["references"]},{"@id":"https://cir.nii.ac.jp/crid/1390001205122245760","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Syntheses and Application of Dibasic Acids Containing Furan or Tetrahydrofuran Ring."},{"@value":"(366)フラン環またはテトラヒドロフラン環を含む二塩基酸の合成とその利用について"}]},{"@id":"https://cir.nii.ac.jp/crid/1390001206287590144","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Room-Temperature Polycondensation of Dicarboxylic Acids and Diols Catalyzed by Water-Stable Lewis Acids"},{"@value":"Room-temperature polycondensation of dicarboxylic acids and diols catalyzed by water-stable Lewis acid"}]},{"@id":"https://cir.nii.ac.jp/crid/1390282680098957568","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Syntheses of Polyesters Containing Furan Ring"},{"@value":"フラン環を含むポリエステルの合成"}]},{"@id":"https://cir.nii.ac.jp/crid/1390282681500993408","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Synthesis of Poly(butylene succinate) Copolymer Including 2,5-Furandicarboxylate"},{"@language":"ja","@value":"２，５－フランジカルボン酸を含有するポリブチレンサクシネートコポリマーの合成"},{"@language":"ja-Kana","@value":"2 5 フランジカルボンサン オ ガンユウ スル ポリブチレンサクシネートコ ポリマー ノ ゴウセイ"}]},{"@id":"https://cir.nii.ac.jp/crid/1570009750615426688","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1570009750615432064","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1570572700568848128","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1570854175545566976","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1572261550429118208","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1572543025405831552","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1573105975359250176","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1573105976512170624","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1573105976562717696","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1573387450335959936","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1573387450335961088","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1573387450335963264","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1573668925312667264","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1573950401496168960","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1574231875266092800","@type":"Article","relationType":["cites"]}],"dataSourceIdentifier":[{"@type":"CROSSREF","@value":"10.1246/cl.2008.50"},{"@type":"CIA","@value":"10020147756"},{"@type":"OPENAIRE","@value":"doi_dedup___::fbb38082bfaed6bc8a9f50ac86b762d4"},{"@type":"CROSSREF","@value":"10.1002/ente.201700404_references_DOI_L1uyrNNHsOLW69pPufXqefjiNDl"},{"@type":"CROSSREF","@value":"10.1295/koron.67.541_references_DOI_L1uyrNNHsOLW69pPufXqefjiNDl"},{"@type":"CROSSREF","@value":"10.1016/j.molcatb.2016.11.021_references_DOI_L1uyrNNHsOLW69pPufXqefjiNDl"}]}