{"@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/1361699995576256256.json","@type":"Article","productIdentifier":[{"identifier":{"@type":"DOI","@value":"10.1002/anie.201208547"}},{"identifier":{"@type":"URI","@value":"https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fanie.201208547"}},{"identifier":{"@type":"URI","@value":"https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.201208547"}}],"dc:title":[{"@value":"The Fold‐In Approach to Bowl‐Shaped Aromatic Compounds: Synthesis of Chrysaoroles"}],"creator":[{"@id":"https://cir.nii.ac.jp/crid/1381699995576256384","@type":"Researcher","foaf:name":[{"@value":"Damian Myśliwiec"}]},{"@id":"https://cir.nii.ac.jp/crid/1381699995576256385","@type":"Researcher","foaf:name":[{"@value":"Marcin Stępień"}]}],"publication":{"publicationIdentifier":[{"@type":"PISSN","@value":"14337851"},{"@type":"EISSN","@value":"15213773"}],"prism:publicationName":[{"@value":"Angewandte Chemie International Edition"}],"dc:publisher":[{"@value":"Wiley"}],"prism:publicationDate":"2012-12-17","prism:volume":"52","prism:number":"6","prism:startingPage":"1713","prism:endingPage":"1717"},"reviewed":"false","dc:rights":["http://onlinelibrary.wiley.com/termsAndConditions#vor"],"url":[{"@id":"https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fanie.201208547"},{"@id":"https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.201208547"}],"createdAt":"2012-12-18","modifiedAt":"2023-10-16","relatedProduct":[{"@id":"https://cir.nii.ac.jp/crid/1050001338813802112","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Synthesis and Size-Dependent Properties of [12], [16], and [24]Carbon Nanobelts"}]},{"@id":"https://cir.nii.ac.jp/crid/1050282813782541696","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Synthesis of a carbon nanobelt"}]},{"@id":"https://cir.nii.ac.jp/crid/1050294872220241664","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Fold‐in Synthesis of a Pentabenzopentaaza[10]circulene"}]},{"@id":"https://cir.nii.ac.jp/crid/1050573243093038592","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Improved Synthesis of ortho-Phenylene-bridged Cyclic Tetrapyrroles and Oxidative Fusion Reactions Toward Substituted Tetraaza[8]circulenes"},{"@value":"Improved Synthesis of <i>ortho</i>‐Phenylene‐bridged Cyclic Tetrapyrroles and Oxidative Fusion Reactions Toward Substituted Tetraaza[8]circulenes"}]},{"@id":"https://cir.nii.ac.jp/crid/1360009142816272128","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Highly Stable Radical Cations of <i>N</i>,<i>N’</i>‐Diarylated Tetrabenzotetraaza[8]circulene"}]},{"@id":"https://cir.nii.ac.jp/crid/1360025430624635776","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Bowl‐Shaped Kekulene Analogues: Cycloarenes with two Five‐Membered Rings"}]},{"@id":"https://cir.nii.ac.jp/crid/1360285704901901824","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Closed Pentaaza[9]helicene and Hexathia[9]/[5]helicene: Oxidative Fusion Reactions of <i>ortho</i>‐Phenylene‐Bridged Cyclic Hexapyrroles and Hexathiophenes"}]},{"@id":"https://cir.nii.ac.jp/crid/1360294643769491584","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Synthesis of octagon-containing molecular nanocarbons"}]},{"@id":"https://cir.nii.ac.jp/crid/1360302864775203200","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Non-Planar Polycyclic Aromatic Molecules Including Heterole Units"}]},{"@id":"https://cir.nii.ac.jp/crid/1360565164378940288","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Functional Sulfur‐Doped Buckybowls and Their Concave–Convex Supramolecular Assembly with Fullerenes"}]},{"@id":"https://cir.nii.ac.jp/crid/1360567179947530752","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Nonplanar Butterfly‐Shaped π‐Expanded Pyrrolopyrroles"}]},{"@id":"https://cir.nii.ac.jp/crid/1360567183095979136","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Unforeseen 1,2-Aryl Shift in Tetraarylpyrrolo[3,2-<i>b</i>]pyrroles Triggered by Oxidative Aromatic Coupling"}]},{"@id":"https://cir.nii.ac.jp/crid/1360567183566976256","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Exploring the “fold-in” strategy toward the construction of a highly-strained triazasumanene skeleton"}]},{"@id":"https://cir.nii.ac.jp/crid/1360574096137908352","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Synthesis of a Tetrabenzotetraaza[8]circulene by a “Fold‐In” Oxidative Fusion Reaction"}]},{"@id":"https://cir.nii.ac.jp/crid/1360576118745981696","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Chemical Synthesis of Carbon Nanorings and Nanobelts"}]},{"@id":"https://cir.nii.ac.jp/crid/1360848654825112576","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"<i>ortho</i>‐Phenylene‐Bridged Hybrid Nanorings of 2,5‐Pyrrolylenes and 2,5‐Thienylenes"}]},{"@id":"https://cir.nii.ac.jp/crid/1360848654925351168","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Non‐Planar [<i>n</i>]Cyclo‐1,8‐carbazolylenes (<i>n=</i>3,4,6) and [3]Cyclo‐1,8‐carbazolylenyl B, P, PO, SiPh Complexes"}]},{"@id":"https://cir.nii.ac.jp/crid/1360848656984050944","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Macrocyclic Polyradicaloids with Unusual Super-ring Structure and Global Aromaticity"}]},{"@id":"https://cir.nii.ac.jp/crid/1360848658146263424","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Fully Fused Quinoidal/Aromatic Carbazole Macrocycles with Poly-radical Characters"}]},{"@id":"https://cir.nii.ac.jp/crid/1360861291386163968","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"N-doped nonalternant aromatic belt\n                    <i>via</i>\n                    a six-fold annulative double N-arylation"}]},{"@id":"https://cir.nii.ac.jp/crid/1360865815499660672","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Isomerism tunes the diradical character of difluorenopyrroles at constant Hückel-level anti-aromaticity"}]},{"@id":"https://cir.nii.ac.jp/crid/1361412892976917760","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Synthesis of Belt- and Möbius-Shaped Cycloparaphenylenes by Rhodium-Catalyzed Alkyne Cyclotrimerization"}]},{"@id":"https://cir.nii.ac.jp/crid/1390565134804298880","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Synthesis and Property of Three-dimensional Curved Heterocyclic π-Electron Molecules with Embedded Nitrogen Atoms"},{"@language":"ja","@value":"含窒素三次元湾曲ヘテロπ電子系分子の合成と性質"},{"@language":"ja-Kana","@value":"ガン チッソ サンジゲン ワンキョク ヘテロpデンシケイ ブンシ ノ ゴウセイ ト セイシツ"}]},{"@id":"https://cir.nii.ac.jp/crid/1390848250127226240","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Synthesis and Properties of Tetraaza［8］circulene and its Analogs"},{"@language":"ja","@value":"テトラアザ［8］サーキュレンおよびその類縁体の合成と物性"},{"@language":"ja-Kana","@value":"テトラアザ[8]サーキュレン オヨビ ソノ ルイエンタイ ノ ゴウセイ ト ブッセイ"}]},{"@id":"https://cir.nii.ac.jp/crid/2051433317038775040","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Synthesis of novel heteronanographenes via fold-in approach"}]}],"dataSourceIdentifier":[{"@type":"CROSSREF","@value":"10.1002/anie.201208547"},{"@type":"CROSSREF","@value":"10.1126/science.aam8158_references_DOI_A0omvH6AR2B4Oiyj4fyECmxB2yy"},{"@type":"CROSSREF","@value":"10.1016/j.chempr.2018.03.020_references_DOI_A0omvH6AR2B4Oiyj4fyECmxB2yy"},{"@type":"CROSSREF","@value":"10.1002/chem.202001934_references_DOI_A0omvH6AR2B4Oiyj4fyECmxB2yy"},{"@type":"CROSSREF","@value":"10.1039/d2sc02647c_references_DOI_A0omvH6AR2B4Oiyj4fyECmxB2yy"},{"@type":"CROSSREF","@value":"10.1002/chem.202401828_references_DOI_A0omvH6AR2B4Oiyj4fyECmxB2yy"},{"@type":"CROSSREF","@value":"10.1002/anie.201708429_references_DOI_A0omvH6AR2B4Oiyj4fyECmxB2yy"},{"@type":"CROSSREF","@value":"10.1021/jacs.9b06197_references_DOI_A0omvH6AR2B4Oiyj4fyECmxB2yy"},{"@type":"CROSSREF","@value":"10.1021/jacs.6b04539_references_DOI_A0omvH6AR2B4Oiyj4fyECmxB2yy"},{"@type":"CROSSREF","@value":"10.1039/d1sc05586k_references_DOI_A0omvH6AR2B4Oiyj4fyECmxB2yy"},{"@type":"CROSSREF","@value":"10.1246/bcsj.20220030_references_DOI_A0omvH6AR2B4Oiyj4fyECmxB2yy"},{"@type":"CROSSREF","@value":"10.3987/rev-22-982_references_DOI_A0omvH6AR2B4Oiyj4fyECmxB2yy"},{"@type":"CROSSREF","@value":"10.1002/anie.201606383_references_DOI_A0omvH6AR2B4Oiyj4fyECmxB2yy"},{"@type":"CROSSREF","@value":"10.1002/chem.201603282_references_DOI_A0omvH6AR2B4Oiyj4fyECmxB2yy"},{"@type":"CROSSREF","@value":"10.1039/c7cc00329c_references_DOI_A0omvH6AR2B4Oiyj4fyECmxB2yy"},{"@type":"CROSSREF","@value":"10.1002/asia.202001459_references_DOI_A0omvH6AR2B4Oiyj4fyECmxB2yy"},{"@type":"CROSSREF","@value":"10.1021/accountsmr.1c00105_references_DOI_A0omvH6AR2B4Oiyj4fyECmxB2yy"},{"@type":"CROSSREF","@value":"10.1002/anie.202116789_references_DOI_A0omvH6AR2B4Oiyj4fyECmxB2yy"},{"@type":"CROSSREF","@value":"10.1002/anie.201505124_references_DOI_A0omvH6AR2B4Oiyj4fyECmxB2yy"},{"@type":"CROSSREF","@value":"10.1002/ajoc.201900168_references_DOI_A0omvH6AR2B4Oiyj4fyECmxB2yy"},{"@type":"CROSSREF","@value":"10.1002/chem.201702853_references_DOI_A0omvH6AR2B4Oiyj4fyECmxB2yy"},{"@type":"CROSSREF","@value":"10.1039/d3sc03297c_references_DOI_A0omvH6AR2B4Oiyj4fyECmxB2yy"},{"@type":"CROSSREF","@value":"10.5059/yukigoseikyokaishi.77.1209_references_DOI_A0omvH6AR2B4Oiyj4fyECmxB2yy"},{"@type":"CROSSREF","@value":"10.1021/acs.orglett.8b00223_references_DOI_A0omvH6AR2B4Oiyj4fyECmxB2yy"},{"@type":"CROSSREF","@value":"10.5059/yukigoseikyokaishi.78.683_references_DOI_A0omvH6AR2B4Oiyj4fyECmxB2yy"},{"@type":"CROSSREF","@value":"10.1021/jacs.8b06842_references_DOI_A0omvH6AR2B4Oiyj4fyECmxB2yy"}]}