{"@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/1361699993468458752.json","@type":"Article","productIdentifier":[{"identifier":{"@type":"DOI","@value":"10.1039/c4np00106k"}},{"identifier":{"@type":"URI","@value":"http://pubs.rsc.org/en/content/articlepdf/2015/NP/C4NP00106K"}}],"dc:title":[{"@value":"Ester coupling reactions – an enduring challenge in the chemical synthesis of bioactive natural products"}],"description":[{"type":"abstract","notation":[{"@value":"<p>In this review we investigate the use of complex ester fragment couplings within natural product total syntheses. Using examples from the literature up to 2014 we illustrate the state-of-the-art as well as the challenges within this area of organic synthesis.</p>"}]}],"creator":[{"@id":"https://cir.nii.ac.jp/crid/1381699993468458755","@type":"Researcher","foaf:name":[{"@value":"Michail Tsakos"}],"jpcoar:affiliationName":[{"@value":"Chemical Biology Laboratory"},{"@value":"Department of Chemistry"},{"@value":"Aarhus University"},{"@value":"Aarhus C"},{"@value":"Denmark"}]},{"@id":"https://cir.nii.ac.jp/crid/1381699993468458752","@type":"Researcher","foaf:name":[{"@value":"Eva S. Schaffert"}],"jpcoar:affiliationName":[{"@value":"Chemical Biology Laboratory"},{"@value":"Department of Chemistry"},{"@value":"Aarhus University"},{"@value":"Aarhus C"},{"@value":"Denmark"}]},{"@id":"https://cir.nii.ac.jp/crid/1381699993468458754","@type":"Researcher","foaf:name":[{"@value":"Lise L. Clement"}],"jpcoar:affiliationName":[{"@value":"Chemical Biology Laboratory"},{"@value":"Department of Chemistry"},{"@value":"Aarhus University"},{"@value":"Aarhus C"},{"@value":"Denmark"}]},{"@id":"https://cir.nii.ac.jp/crid/1381699993468458753","@type":"Researcher","foaf:name":[{"@value":"Nikolaj L. Villadsen"}],"jpcoar:affiliationName":[{"@value":"Chemical Biology Laboratory"},{"@value":"Department of Chemistry"},{"@value":"Aarhus University"},{"@value":"Aarhus C"},{"@value":"Denmark"}]},{"@id":"https://cir.nii.ac.jp/crid/1381699993468458756","@type":"Researcher","foaf:name":[{"@value":"Thomas B. Poulsen"}],"jpcoar:affiliationName":[{"@value":"Chemical Biology Laboratory"},{"@value":"Department of Chemistry"},{"@value":"Aarhus University"},{"@value":"Aarhus C"},{"@value":"Denmark"}]}],"publication":{"publicationIdentifier":[{"@type":"PISSN","@value":"02650568"},{"@type":"EISSN","@value":"14604752"}],"prism:publicationName":[{"@value":"Natural Product Reports"}],"dc:publisher":[{"@value":"Royal Society of Chemistry (RSC)"}],"prism:publicationDate":"2015","prism:volume":"32","prism:number":"4","prism:startingPage":"605","prism:endingPage":"632"},"reviewed":"false","url":[{"@id":"http://pubs.rsc.org/en/content/articlepdf/2015/NP/C4NP00106K"}],"createdAt":"2015-01-09","modifiedAt":"2024-04-17","relatedProduct":[{"@id":"https://cir.nii.ac.jp/crid/1050305024802347520","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"RNA-dependent synthesis of ergosteryl-3β-O-glycine in Ascomycota expands the diversity of steryl-amino acids"}]},{"@id":"https://cir.nii.ac.jp/crid/1050587981429132288","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Further applications of classical amide coupling reagents: Microwave-assisted esterification on solid phase"},{"@value":"Further applications of classical amide coupling reagents: Microwave‐assisted esterification on solid phase"}]},{"@id":"https://cir.nii.ac.jp/crid/1360004233131208832","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Total Synthesis and Stereochemical Revision of Stereocalpin A: Mirror-Image Approach for Stereochemical Assignments of the Peptide–Polyketide Macrocycle"}]},{"@id":"https://cir.nii.ac.jp/crid/1360005516642874240","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Quantitative analysis of native reactive functional groups on carbon fiber surface: An electrochemical approach"}]},{"@id":"https://cir.nii.ac.jp/crid/1360846641543026688","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Total Synthesis of Theonellapeptolide Id"}]},{"@id":"https://cir.nii.ac.jp/crid/1360857593734351104","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Development of a triazinedione-based dehydrative condensing reagent containing 4-(dimethylamino)pyridine as an acyl transfer catalyst"}]}],"dataSourceIdentifier":[{"@type":"CROSSREF","@value":"10.1039/c4np00106k"},{"@type":"CROSSREF","@value":"10.1002/psc.3111_references_DOI_2MiYktv2RIGinkae06QEVwLMnxv"},{"@type":"CROSSREF","@value":"10.1016/j.apsusc.2019.07.185_references_DOI_2MiYktv2RIGinkae06QEVwLMnxv"},{"@type":"CROSSREF","@value":"10.1016/j.jbc.2022.101657_references_DOI_2MiYktv2RIGinkae06QEVwLMnxv"},{"@type":"CROSSREF","@value":"10.1039/d1ob00450f_references_DOI_2MiYktv2RIGinkae06QEVwLMnxv"},{"@type":"CROSSREF","@value":"10.1021/acs.orglett.7b00249_references_DOI_2MiYktv2RIGinkae06QEVwLMnxv"},{"@type":"CROSSREF","@value":"10.1021/acs.joc.8b00118_references_DOI_2MiYktv2RIGinkae06QEVwLMnxv"}]}