{"@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/1363670320927196288.json","@type":"Article","productIdentifier":[{"identifier":{"@type":"DOI","@value":"10.1002/ange.201209060"}},{"identifier":{"@type":"URI","@value":"https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fange.201209060"}},{"identifier":{"@type":"URI","@value":"https://onlinelibrary.wiley.com/doi/pdf/10.1002/ange.201209060"}}],"dc:title":[{"@value":"Organische Elektronendonoren als leistungsfähige Ein‐Elektronen‐Reduktionsmittel in der organischen Synthese"}],"description":[{"type":"abstract","notation":[{"@value":"<jats:title>Abstract</jats:title><jats:p>In der organischen Chemie wird die Ein‐Elektronen‐Reduktion häufig verwendet, um eine Radikalbildung durch den schrittweisen Transfer von einem oder zwei Elektronen von einem Donor auf ein organisches Substrat zu realisieren. Neben den metallischen Reagentien haben sich Reduktionsmittel auf der Basis neutraler organischer Moleküle, die einen Ein‐Elektronen‐Transfer ermöglichen, als eine attraktive neue Quelle für reduzierende Elektronen erwiesen. In den letzten zwanzig Jahren ist eine besondere Klasse organischer Reduktionsmittel, die elektronenreichen Olefine, zunehmend in Erscheinung getreten, und ihre Anwendung in der organischen Synthese hat sich vervielfacht. In diesem Aufsatz werden die verschiedenen Arten von organischen Donoren und ihre spezifischen Besonderheiten in organischen Umwandlungen zusammengefasst und diskutiert.</jats:p>"}]}],"creator":[{"@id":"https://cir.nii.ac.jp/crid/1383670320927196160","@type":"Researcher","foaf:name":[{"@value":"Julie Broggi"}]},{"@id":"https://cir.nii.ac.jp/crid/1383670320927196161","@type":"Researcher","foaf:name":[{"@value":"Thierry Terme"}]},{"@id":"https://cir.nii.ac.jp/crid/1383670320927196288","@type":"Researcher","foaf:name":[{"@value":"Patrice Vanelle"}]}],"publication":{"publicationIdentifier":[{"@type":"PISSN","@value":"00448249"},{"@type":"EISSN","@value":"15213757"}],"prism:publicationName":[{"@value":"Angewandte Chemie"}],"dc:publisher":[{"@value":"Wiley"}],"prism:publicationDate":"2013-11-24","prism:volume":"126","prism:number":"2","prism:startingPage":"392","prism:endingPage":"423"},"reviewed":"false","dc:rights":["http://onlinelibrary.wiley.com/termsAndConditions#vor"],"url":[{"@id":"https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fange.201209060"},{"@id":"https://onlinelibrary.wiley.com/doi/pdf/10.1002/ange.201209060"}],"createdAt":"2013-11-25","modifiedAt":"2023-10-17","relatedProduct":[{"@id":"https://cir.nii.ac.jp/crid/1360004229993037952","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Synthesis of Three‐Dimensional Butterfly Slit‐Cyclobisazaanthracenes and Hydrazinobisanthenes through One‐Step Cyclodimerization and Their Properties"}]},{"@id":"https://cir.nii.ac.jp/crid/1360013168888101760","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Synthesis and Characterization of 16π Antiaromatic 2,7‐Dihydrodiazapyrenes: Antiaromatic Polycyclic Hydrocarbons with Embedded Nitrogen"}]},{"@id":"https://cir.nii.ac.jp/crid/1360567179876650368","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Switchover of the Mechanism between Electron Transfer and Hydrogen‐Atom Transfer for a Protonated Manganese(IV)–Oxo Complex by Changing Only the Reaction Temperature"}]}],"dataSourceIdentifier":[{"@type":"CROSSREF","@value":"10.1002/ange.201209060"},{"@type":"CROSSREF","@value":"10.1002/chem.201504144_references_DOI_YjlbEguNbPGKwkfV3A3TJrbOF0W"},{"@type":"CROSSREF","@value":"10.1002/anie.202103667_references_DOI_YjlbEguNbPGKwkfV3A3TJrbOF0W"},{"@type":"CROSSREF","@value":"10.1002/anie.201602460_references_DOI_YjlbEguNbPGKwkfV3A3TJrbOF0W"}]}