{"@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/1362262944817334528.json","@type":"Article","productIdentifier":[{"identifier":{"@type":"DOI","@value":"10.1021/cr500523x"}},{"identifier":{"@type":"URI","@value":"https://pubs.acs.org/doi/pdf/10.1021/cr500523x"}}],"dc:title":[{"@value":"Cubane: 50 Years Later"}],"creator":[{"@id":"https://cir.nii.ac.jp/crid/1382262944817334530","@type":"Researcher","foaf:name":[{"@value":"Kyle F. Biegasiewicz"}],"jpcoar:affiliationName":[{"@value":"Department of Chemistry, University of Rochester, Rochester, New York 14627-0216, United States"}]},{"@id":"https://cir.nii.ac.jp/crid/1382262944817334529","@type":"Researcher","foaf:name":[{"@value":"Justin R. Griffiths"}],"jpcoar:affiliationName":[{"@value":"Department of Chemistry, University at Buffalo, Buffalo, New York 14260-1660, United States"}]},{"@id":"https://cir.nii.ac.jp/crid/1382262944817334531","@type":"Researcher","foaf:name":[{"@value":"G. Paul Savage"}],"jpcoar:affiliationName":[{"@value":"Ian Wark Laboratory, CSIRO Manufacturing Flagship, Bayview Avenue, Clayton, Victoria 3168, Australia"}]},{"@id":"https://cir.nii.ac.jp/crid/1382262944817334528","@type":"Researcher","foaf:name":[{"@value":"John Tsanaktsidis"}],"jpcoar:affiliationName":[{"@value":"Ian Wark Laboratory, CSIRO Manufacturing Flagship, Bayview Avenue, Clayton, Victoria 3168, Australia"}]},{"@id":"https://cir.nii.ac.jp/crid/1382262944817334532","@type":"Researcher","foaf:name":[{"@value":"Ronny Priefer"}],"jpcoar:affiliationName":[{"@value":"College of Pharmacy, Western New England University, Springfield, Massachusetts 01119, United States"}]}],"publication":{"publicationIdentifier":[{"@type":"PISSN","@value":"00092665"},{"@type":"EISSN","@value":"15206890"}],"prism:publicationName":[{"@value":"Chemical Reviews"}],"dc:publisher":[{"@value":"American Chemical Society (ACS)"}],"prism:publicationDate":"2015-06-23","prism:volume":"115","prism:number":"14","prism:startingPage":"6719","prism:endingPage":"6745"},"reviewed":"false","url":[{"@id":"https://pubs.acs.org/doi/pdf/10.1021/cr500523x"}],"createdAt":"2015-06-23","modifiedAt":"2024-06-09","relatedProduct":[{"@id":"https://cir.nii.ac.jp/crid/1050585493123883392","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"How to Set the “Chirality” of Polyhedral Small Molecule Hydrocarbons: Decoration and Editing of Cubane Skeleton"}]},{"@id":"https://cir.nii.ac.jp/crid/1050585559409991936","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Scaffold Editing of Cubanes into Homocubanes, Homocuneanes via Cuneanes"}]},{"@id":"https://cir.nii.ac.jp/crid/1050856660844282880","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Catalytic Asymmetric Synthesis of 2,6‐Disubstituted Cuneanes via Enantioselective Constitutional Isomerization of 1,4‐Disubstituted Cubanes"},{"@value":"Catalytic Asymmetric Synthesis of 2,6‐Disubstituted Cuneanes through Enantioselective Constitutional Isomerization of 1,4‐Disubstituted Cubanes"}]},{"@id":"https://cir.nii.ac.jp/crid/1360013168785644800","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"<i>ortho</i>-C–H Acetoxylation of Cubane Enabling Access to Cubane Analogues of Pharmaceutically Relevant Scaffolds"}]},{"@id":"https://cir.nii.ac.jp/crid/1360017279837076736","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Electron in a cube: Synthesis and characterization of perfluorocubane as an electron acceptor"}]},{"@id":"https://cir.nii.ac.jp/crid/1360025429420218880","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Asymmetric Synthesis of Noradamantane Scaffolds via Diphenylprolinol Silyl Ether‐Mediated Domino Michael/Epimerization/Michael (or Aldol)/1,2‐Addition Reactions"}]},{"@id":"https://cir.nii.ac.jp/crid/1360285706151442816","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Substituent effects in cubane and hypercubane: a DFT and QTAIM study"}]},{"@id":"https://cir.nii.ac.jp/crid/1360285708119513984","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"A Protocol for an Iodine–Metal Exchange Reaction on Cubane Using Lithium Organozincates"}]},{"@id":"https://cir.nii.ac.jp/crid/1360298337126967808","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Directed Metalation of 1-Cuneanecarboxamide: Simple Route to 1,2-Disubstituted Cuneanes"}]},{"@id":"https://cir.nii.ac.jp/crid/1360298341430199424","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Chiral Auxiliary-Directed Site-Selective Deprotonation of the Cubane Skeleton"}]},{"@id":"https://cir.nii.ac.jp/crid/1360302865555853312","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"C–H Alkylation of Cubanes via Catalytic Generation of Cubyl Radicals"}]},{"@id":"https://cir.nii.ac.jp/crid/1360306906087921664","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Recent Progress in Accessing Multi-functionalized Caged Hydrocarbons: En Route to Highly Functionalized Saturated (Bio)isosteres of Benzene Rings"}]},{"@id":"https://cir.nii.ac.jp/crid/1360576121598039424","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Unmasking Inherent Chirality within the Cubane Skeleton"}]},{"@id":"https://cir.nii.ac.jp/crid/1360584341819092096","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Biological Evaluation of Isosteric Applicability of 1,3‐Substituted Cuneanes as <i>m</i>‐Substituted Benzenes Enabled by Selective Isomerization of 1,4‐Substituted Cubanes"}]},{"@id":"https://cir.nii.ac.jp/crid/1360853567643792128","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Programmable synthesis of multiply arylated cubanes through C–H metalation and arylation"}]},{"@id":"https://cir.nii.ac.jp/crid/1360853567705410304","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Decarboxylative Bromination of Sterically Hindered Carboxylic Acids with Hypervalent Iodine(III) Reagents"}]},{"@id":"https://cir.nii.ac.jp/crid/1360865814731655936","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Decoration on Cubane with an Awareness of Chirality: Development of Substituted Cubane Syntheses"}]},{"@id":"https://cir.nii.ac.jp/crid/1360865814732395904","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Constitutional isomerization of cubane to semibullvalene via cuneane in hot water"}]},{"@id":"https://cir.nii.ac.jp/crid/1360869856034037504","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Strategy for C−H Functionalization of Cubanes: From Stoichiometric Reaction to Catalytic Methodology"}]},{"@id":"https://cir.nii.ac.jp/crid/1361694368372426112","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Organocopper cross-coupling reaction for C–C bond formation on highly sterically hindered structures"}]},{"@id":"https://cir.nii.ac.jp/crid/1361975842845956352","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Cubane Chirality via Substitution of a “Hidden” Regular Tetrahedron"}]},{"@id":"https://cir.nii.ac.jp/crid/1390023936882379264","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Amide-Directed C–H Acetoxylation of Cubanes"}]},{"@id":"https://cir.nii.ac.jp/crid/1390302845892547584","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Comprehensive Synthesis of a Group of Optically Active Caged Hydrocarbon Molecules—Cubane Scaffold Editing—"},{"@language":"ja","@value":"光学活性かご型炭化水素分子群の網羅的合成—キュバンScaffold Editing—"}]},{"@id":"https://cir.nii.ac.jp/crid/2050588892112986880","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Studies for absolute configuration of chiral 2,6-cuneanedicarboxylic acid esters"}]}],"dataSourceIdentifier":[{"@type":"CROSSREF","@value":"10.1021/cr500523x"},{"@type":"CROSSREF","@value":"10.1021/acs.orglett.1c03144_references_DOI_TU4krhM3FJgPDy4hrosevK9VwWG"},{"@type":"CROSSREF","@value":"10.1021/acs.orglett.2c03659_references_DOI_TU4krhM3FJgPDy4hrosevK9VwWG"},{"@type":"CROSSREF","@value":"10.1126/science.abq0516_references_DOI_TU4krhM3FJgPDy4hrosevK9VwWG"},{"@type":"CROSSREF","@value":"10.1002/ejoc.202200567_references_DOI_TU4krhM3FJgPDy4hrosevK9VwWG"},{"@type":"CROSSREF","@value":"10.1248/cpb.c25-00449_references_DOI_TU4krhM3FJgPDy4hrosevK9VwWG"},{"@type":"CROSSREF","@value":"10.1002/anie.202500378_references_DOI_TU4krhM3FJgPDy4hrosevK9VwWG"},{"@type":"CROSSREF","@value":"10.1007/s00214-017-2144-5_references_DOI_TU4krhM3FJgPDy4hrosevK9VwWG"},{"@type":"CROSSREF","@value":"10.1021/acs.orglett.8b03721_references_DOI_TU4krhM3FJgPDy4hrosevK9VwWG"},{"@type":"CROSSREF","@value":"10.1246/cl.230101_references_DOI_TU4krhM3FJgPDy4hrosevK9VwWG"},{"@type":"CROSSREF","@value":"10.1021/acs.orglett.3c04019_references_DOI_TU4krhM3FJgPDy4hrosevK9VwWG"},{"@type":"CROSSREF","@value":"10.1002/ejoc.202300891_references_DOI_TU4krhM3FJgPDy4hrosevK9VwWG"},{"@type":"CROSSREF","@value":"10.5059/yukigoseikyokaishi.83.46_references_DOI_TU4krhM3FJgPDy4hrosevK9VwWG"},{"@type":"CROSSREF","@value":"10.1055/a-2360-8218_references_DOI_TU4krhM3FJgPDy4hrosevK9VwWG"},{"@type":"CROSSREF","@value":"10.1021/acs.orglett.0c01142_references_DOI_TU4krhM3FJgPDy4hrosevK9VwWG"},{"@type":"CROSSREF","@value":"10.1002/ijch.202100013_references_DOI_TU4krhM3FJgPDy4hrosevK9VwWG"},{"@type":"CROSSREF","@value":"10.1002/chem.202303548_references_DOI_TU4krhM3FJgPDy4hrosevK9VwWG"},{"@type":"CROSSREF","@value":"10.1039/d0sc01909g_references_DOI_TU4krhM3FJgPDy4hrosevK9VwWG"},{"@type":"CROSSREF","@value":"10.1021/acs.oprd.0c00130_references_DOI_TU4krhM3FJgPDy4hrosevK9VwWG"},{"@type":"CROSSREF","@value":"10.1246/cl.220197_references_DOI_TU4krhM3FJgPDy4hrosevK9VwWG"},{"@type":"CROSSREF","@value":"10.1002/chem.202303063_references_DOI_TU4krhM3FJgPDy4hrosevK9VwWG"},{"@type":"CROSSREF","@value":"10.1055/a-2124-3823_references_DOI_TU4krhM3FJgPDy4hrosevK9VwWG"},{"@type":"CROSSREF","@value":"10.1093/chemle/upad010_references_DOI_TU4krhM3FJgPDy4hrosevK9VwWG"},{"@type":"CROSSREF","@value":"10.1002/ejoc.202401055_references_DOI_TU4krhM3FJgPDy4hrosevK9VwWG"},{"@type":"CROSSREF","@value":"10.1039/c9sc00891h_references_DOI_TU4krhM3FJgPDy4hrosevK9VwWG"}]}