{"@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/1361975842845956352.json","@type":"Article","productIdentifier":[{"identifier":{"@type":"DOI","@value":"10.1021/acs.orglett.0c01142"}},{"identifier":{"@type":"URI","@value":"https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.0c01142"}},{"identifier":{"@type":"PMID","@value":"32437157"}}],"resourceType":"学術雑誌論文(journal article)","dc:title":[{"@value":"Cubane Chirality via Substitution of a “Hidden” Regular Tetrahedron"}],"description":[{"notation":[{"@value":"In the hexahedral hydrocarbon cubane, replacing hydrogen with other atoms at three positions within any one of the internal tetrahedrons can conceptually lead to the formation of a unique class of chiral molecules. In pursuit of this endeavor, we prepared 1,3-dibromo-4-deuteriocubane-"}]}],"creator":[{"@id":"https://cir.nii.ac.jp/crid/1381975842845956358","@type":"Researcher","foaf:name":[{"@value":"Nana Yoshino"}],"jpcoar:affiliationName":[{"@value":"Department of Material Chemistry, Graduate School of Engineering, Kyoto University, Kyotodaigaku-Katsura, Nishikyo, Kyoto 615-8510, Japan"}]},{"@id":"https://cir.nii.ac.jp/crid/1381975842845956357","@type":"Researcher","foaf:name":[{"@value":"Yumi Kato"}],"jpcoar:affiliationName":[{"@value":"Department of Material Chemistry, Graduate School of Engineering, Kyoto University, Kyotodaigaku-Katsura, Nishikyo, Kyoto 615-8510, Japan"}]},{"@id":"https://cir.nii.ac.jp/crid/1381975842845956355","@type":"Researcher","foaf:name":[{"@value":"Thibaud Mabit"}],"jpcoar:affiliationName":[{"@value":"JSPS International Fellowship for Research, Department of Material Chemistry, Graduate School of Engineering, Kyoto University, Kyotodaigaku-Katsura, Nishikyo, Kyoto 615-8530, Japan"}]},{"@id":"https://cir.nii.ac.jp/crid/1381975842845956356","@type":"Researcher","foaf:name":[{"@value":"Yuuya Nagata"}],"jpcoar:affiliationName":[{"@value":"Institute for Chemical Reaction Design and Discovery, Hokkaido University, Nishi 10, Kita, Sapporo 001-0021, Japan"}]},{"@id":"https://cir.nii.ac.jp/crid/1381975842845956353","@type":"Researcher","foaf:name":[{"@value":"Craig M. Williams"}],"jpcoar:affiliationName":[{"@value":"School of Chemistry and Molecular Biosciences, University of Queensland, Brisbane, Queensland 4072, Australia"}]},{"@id":"https://cir.nii.ac.jp/crid/1381975842845956354","@type":"Researcher","foaf:name":[{"@value":"Mei Harada"}],"jpcoar:affiliationName":[{"@value":"Graduate School of Pharmaceutical Sciences, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan"}]},{"@id":"https://cir.nii.ac.jp/crid/1381975842845956352","@type":"Researcher","foaf:name":[{"@value":"Atsuya Muranaka"}],"jpcoar:affiliationName":[{"@value":"Cluster of Pioneering Research (CPR), Advanced Elements Chemistry Laboratory, RIKEN, 2-1 Hirosawa, Wako-shi, Saitama 351-0198, Japan"}]},{"@id":"https://cir.nii.ac.jp/crid/1420845751134949888","@type":"Researcher","personIdentifier":[{"@type":"KAKEN_RESEARCHERS","@value":"00271916"},{"@type":"NRID","@value":"1000000271916"},{"@type":"NRID","@value":"9000413774212"},{"@type":"NRID","@value":"9000005267903"},{"@type":"NRID","@value":"9000412056427"},{"@type":"NRID","@value":"9000258598299"},{"@type":"NRID","@value":"9000257821541"},{"@type":"NRID","@value":"9000252119933"},{"@type":"NRID","@value":"9000365541802"},{"@type":"NRID","@value":"9000412115352"},{"@type":"NRID","@value":"9000410198563"},{"@type":"NRID","@value":"9000257734166"},{"@type":"NRID","@value":"9000347641688"},{"@type":"NRID","@value":"9000283394904"},{"@type":"NRID","@value":"9000263039214"},{"@type":"NRID","@value":"9000408915567"},{"@type":"NRID","@value":"9000002045392"},{"@type":"NRID","@value":"9000307260969"},{"@type":"NRID","@value":"9000326650689"},{"@type":"NRID","@value":"9000241847459"},{"@type":"NRID","@value":"9000413946953"},{"@type":"NRID","@value":"9000254711986"},{"@type":"NRID","@value":"9000329892775"},{"@type":"NRID","@value":"9000018717895"},{"@type":"NRID","@value":"9000002099390"},{"@type":"NRID","@value":"9000411022759"},{"@type":"NRID","@value":"9000413895118"},{"@type":"NRID","@value":"9000406378838"},{"@type":"RESEARCHMAP","@value":"https://researchmap.jp/read0184545"}],"foaf:name":[{"@value":"Masanobu Uchiyama"}],"jpcoar:affiliationName":[{"@value":"Graduate School of Pharmaceutical Sciences, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan"},{"@value":"Cluster of Pioneering Research (CPR), Advanced Elements Chemistry Laboratory, RIKEN, 2-1 Hirosawa, Wako-shi, Saitama 351-0198, Japan"}]},{"@id":"https://cir.nii.ac.jp/crid/1420845751166909312","@type":"Researcher","personIdentifier":[{"@type":"KAKEN_RESEARCHERS","@value":"90190496"},{"@type":"NRID","@value":"1000090190496"},{"@type":"ORCID","@value":"0000-0001-8484-4574"},{"@type":"CINII_AUTHOR_ID","@value":"DA17554299"},{"@type":"URI","@value":"https://ci.nii.ac.jp/author/DA17554299#entity"},{"@type":"URI","@value":"https://viaf.org/viaf/NII%7CDA17554299"},{"@type":"NRID","@value":"9000000826358"},{"@type":"NRID","@value":"9000001995925"},{"@type":"NRID","@value":"9000259336382"},{"@type":"NRID","@value":"9000265565329"},{"@type":"NRID","@value":"9000257734898"},{"@type":"NRID","@value":"9000265565326"},{"@type":"NRID","@value":"9000020138474"},{"@type":"NRID","@value":"9000347276612"},{"@type":"NRID","@value":"9000272989524"},{"@type":"NRID","@value":"9000001283991"},{"@type":"NRID","@value":"9000018233569"},{"@type":"NRID","@value":"9000021898607"},{"@type":"NRID","@value":"9000257734789"},{"@type":"NRID","@value":"9000257719208"},{"@type":"NRID","@value":"9000007271258"},{"@type":"NRID","@value":"9000020288505"},{"@type":"NRID","@value":"9000021901379"},{"@type":"NRID","@value":"9000021857474"},{"@type":"NRID","@value":"9000293833404"},{"@type":"NRID","@value":"9000257733748"},{"@type":"NRID","@value":"9000257730481"},{"@type":"NRID","@value":"9000394960025"},{"@type":"NRID","@value":"9000019143446"},{"@type":"NRID","@value":"9000018651133"},{"@type":"NRID","@value":"9000257732891"},{"@type":"NRID","@value":"9000000262981"},{"@type":"NRID","@value":"9000021887464"},{"@type":"NRID","@value":"9000021871204"},{"@type":"NRID","@value":"9000283388390"},{"@type":"NRID","@value":"9000257722181"},{"@type":"NRID","@value":"9000257717061"},{"@type":"NRID","@value":"9000009217303"},{"@type":"NRID","@value":"9000000540780"},{"@type":"NRID","@value":"9000000842199"},{"@type":"NRID","@value":"9000018232513"},{"@type":"NRID","@value":"9000379609746"},{"@type":"NRID","@value":"9000387366518"},{"@type":"NRID","@value":"9000257701687"},{"@type":"NRID","@value":"9000257727683"},{"@type":"NRID","@value":"9000016324672"},{"@type":"NRID","@value":"9000242109263"},{"@type":"NRID","@value":"9000020192955"},{"@type":"NRID","@value":"9000257724079"},{"@type":"NRID","@value":"9000257723394"},{"@type":"NRID","@value":"9000018795750"},{"@type":"NRID","@value":"9000258731245"},{"@type":"NRID","@value":"9000264550496"},{"@type":"NRID","@value":"9000021409180"},{"@type":"NRID","@value":"9000411624071"},{"@type":"NRID","@value":"9000257722121"},{"@type":"NRID","@value":"9000256905455"},{"@type":"NRID","@value":"9000408918245"},{"@type":"NRID","@value":"9000257721595"},{"@type":"NRID","@value":"9000257713741"},{"@type":"NRID","@value":"9000410345090"},{"@type":"NRID","@value":"9000257840425"},{"@type":"NRID","@value":"9000257733796"},{"@type":"NRID","@value":"9000018556003"},{"@type":"NRID","@value":"9000370763463"},{"@type":"NRID","@value":"9000378659455"},{"@type":"NRID","@value":"9000016385110"},{"@type":"NRID","@value":"9000310741608"},{"@type":"NRID","@value":"9000276429841"},{"@type":"NRID","@value":"9000021829270"},{"@type":"NRID","@value":"9000257705579"},{"@type":"NRID","@value":"9000257715829"},{"@type":"NRID","@value":"9000257733330"},{"@type":"NRID","@value":"9000000545293"},{"@type":"NRID","@value":"9000257722629"},{"@type":"NRID","@value":"9000257733260"},{"@type":"NRID","@value":"9000000872948"},{"@type":"NRID","@value":"9000240539165"},{"@type":"NRID","@value":"9000257729504"},{"@type":"NRID","@value":"9000399607702"},{"@type":"NRID","@value":"9000019108884"},{"@type":"NRID","@value":"9000246812957"},{"@type":"NRID","@value":"9000018718011"},{"@type":"NRID","@value":"9000002107358"},{"@type":"NRID","@value":"9000237870074"},{"@type":"NRID","@value":"9000021833026"},{"@type":"NRID","@value":"9000256020471"},{"@type":"RESEARCHMAP","@value":"https://researchmap.jp/read0012787"}],"foaf:name":[{"@value":"Seijiro Matsubara"}],"jpcoar:affiliationName":[{"@value":"Department of Material Chemistry, Graduate School of Engineering, Kyoto University, Kyotodaigaku-Katsura, Nishikyo, Kyoto 615-8510, Japan"}]}],"publication":{"publicationIdentifier":[{"@type":"PISSN","@value":"15237060"},{"@type":"EISSN","@value":"15237052"}],"prism:publicationName":[{"@value":"Organic Letters"}],"dc:publisher":[{"@value":"American Chemical Society (ACS)"}],"prism:publicationDate":"2020-05-21","prism:volume":"22","prism:number":"11","prism:startingPage":"4083","prism:endingPage":"4087"},"reviewed":"false","dc:rights":["https://doi.org/10.15223/policy-029","https://doi.org/10.15223/policy-037","https://doi.org/10.15223/policy-045"],"url":[{"@id":"https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.0c01142"}],"createdAt":"2020-05-21","modifiedAt":"2023-04-15","foaf:topic":[{"@id":"https://cir.nii.ac.jp/all?q=1303%20Biochemistry","dc:title":"1303 Biochemistry"},{"@id":"https://cir.nii.ac.jp/all?q=Organic%20Chemistry","dc:title":"Organic Chemistry"},{"@id":"https://cir.nii.ac.jp/all?q=Physical%20and%20Theoretical%20Chemistry","dc:title":"Physical and Theoretical Chemistry"},{"@id":"https://cir.nii.ac.jp/all?q=1606%20Physical%20and%20Theoretical%20Chemistry","dc:title":"1606 Physical and Theoretical Chemistry"},{"@id":"https://cir.nii.ac.jp/all?q=Biochemistry","dc:title":"Biochemistry"},{"@id":"https://cir.nii.ac.jp/all?q=1605%20Organic%20Chemistry","dc:title":"1605 Organic Chemistry"}],"project":[{"@id":"https://cir.nii.ac.jp/crid/1040000781833978368","@type":"Project","projectIdentifier":[{"@type":"KAKEN","@value":"15H05845"},{"@type":"JGN","@value":"JP15H05845"},{"@type":"URI","@value":"https://kaken.nii.ac.jp/grant/KAKENHI-PLANNED-15H05845/"}],"notation":[{"@language":"ja","@value":"非平衡開放系を利用する反応集積化による精密合成反応の開発"},{"@language":"en","@value":"Development of precise synthetic reaction by reaction integration using a dissipative structure system"}]},{"@id":"https://cir.nii.ac.jp/crid/1040282256936116864","@type":"Project","projectIdentifier":[{"@type":"KAKEN","@value":"17H06173"},{"@type":"JGN","@value":"JP17H06173"},{"@type":"URI","@value":"https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-17H06173/"}],"notation":[{"@language":"ja","@value":"物質と生命を光でつなぐ分子技術の開発"},{"@language":"en","@value":"New Molecular Technologies to Open Up Multiple Applications of Light in Life Science and Materials Science"}]}],"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/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/1360004233216974080","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Radical Multicomponent Carboamination of [1.1.1]Propellane"}]},{"@id":"https://cir.nii.ac.jp/crid/1360011143909749120","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Pharmaceuticals that contain polycyclic hydrocarbon scaffolds"}]},{"@id":"https://cir.nii.ac.jp/crid/1360011145451814912","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Dimerization of Cubene. 1-Iodoadamantane as a Probe for Radical Intermediates"}]},{"@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/1360285708119513984","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"A Protocol for an Iodine–Metal Exchange Reaction on Cubane Using Lithium Organozincates"}]},{"@id":"https://cir.nii.ac.jp/crid/1360292619846906368","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"A REKS Assessment of the Face‐Diagonal Bond in 1,3‐Didehydrocubane and a Comparison with Benzyne Biradicals"}]},{"@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/1360574095292839168","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Validating Eaton's Hypothesis: Cubane as a Benzene Bioisostere"}]},{"@id":"https://cir.nii.ac.jp/crid/1360574096409075968","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Dimethyl Cubane-1,4-dicarboxylate: A Practical Laboratory Scale Synthesis"}]},{"@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/1360584750202333824","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Cuneanes as Potential Benzene Bioisosteres Having Chirality"}]},{"@id":"https://cir.nii.ac.jp/crid/1360853567643792128","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Programmable synthesis of multiply arylated cubanes through C–H metalation and arylation"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855569474407168","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"The reactions of 1,4-dihalocubanes with organolithiums. The case for 1,4-cubadiyl"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855569665889152","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Nonconjugated Hydrocarbons as Rigid‐Linear Motifs: Isosteres for Material Sciences and Bioorganic and Medicinal Chemistry"}]},{"@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/1361137046347375744","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Cubanes in Medicinal Chemistry: Synthesis of Functionalized Building Blocks"}]},{"@id":"https://cir.nii.ac.jp/crid/1361418519759847168","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Escape from Flatland 2: complexity and promiscuity"}]},{"@id":"https://cir.nii.ac.jp/crid/1361418520553531136","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Cubanes: Starting Materials for the Chemistry of the 1990s and the New Century"}]},{"@id":"https://cir.nii.ac.jp/crid/1361418520951072768","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"The Inverted Bond in [1.1.1]Propellane is a Charge‐Shift Bond"}]},{"@id":"https://cir.nii.ac.jp/crid/1361418521392686080","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Toward a Protecting-Group-Free Halogen−Metal Exchange Reaction:  Practical, Chemoselective Metalation of Functionalized Aromatic Halides Using Dianion-type Zincate, <i><sup>t</sup></i>Bu<sub>4</sub>ZnLi<sub>2</sub>"}]},{"@id":"https://cir.nii.ac.jp/crid/1361699995159814784","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Saturated bioisosteres of benzene: where to go next?"}]},{"@id":"https://cir.nii.ac.jp/crid/1361699995357947136","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Function through Synthesis-Informed Design"}]},{"@id":"https://cir.nii.ac.jp/crid/1361981470399882240","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Pharmacophore modeling and applications in drug discovery: challenges and recent advances"}]},{"@id":"https://cir.nii.ac.jp/crid/1362262944807868928","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"The Cubane System"}]},{"@id":"https://cir.nii.ac.jp/crid/1362262944817334528","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Cubane: 50 Years Later"}]},{"@id":"https://cir.nii.ac.jp/crid/1362544421266732928","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Building with Cubane-1,4-diyl. Synthesis of Aryl-Substituted Cubanes, <i>p</i>-[<i>n</i>]Cubyls, and Cubane-Separated Bis(arenes)<sup>1</sup>"}]},{"@id":"https://cir.nii.ac.jp/crid/1362544421273422336","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Strain-Release Heteroatom Functionalization: Development, Scope, and Stereospecificity"}]},{"@id":"https://cir.nii.ac.jp/crid/1362825893331266176","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Site-Selective Aliphatic C–H Bromination Using <i>N</i>-Bromoamides and Visible Light"}]},{"@id":"https://cir.nii.ac.jp/crid/1362825894523927552","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Synopsis of Some Recent Tactical Application of Bioisosteres in Drug Design"}]},{"@id":"https://cir.nii.ac.jp/crid/1362825894524581248","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"On the Discovery of Direct Ortho‐Magnesiation"}]},{"@id":"https://cir.nii.ac.jp/crid/1362825895096593408","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Ab initio calculations of the relative energies of 1,2-, 1,3-, and 1,4-dehydrocubane: prediction of dominant through-bond interaction in 1,4-dehydrocubane"}]},{"@id":"https://cir.nii.ac.jp/crid/1362825896249054336","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Cubanes in Medicinal Chemistry"}]},{"@id":"https://cir.nii.ac.jp/crid/1363107368379145856","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Systematic Enumeration and Symmetries of Cubane Derivatives"}]},{"@id":"https://cir.nii.ac.jp/crid/1363107368412748672","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Systematic substitution on the cubane nucleus. Amide activation for metalation of \"saturated\" systems"}]},{"@id":"https://cir.nii.ac.jp/crid/1363107368838134400","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"The Bent Bonds of Cubane"}]},{"@id":"https://cir.nii.ac.jp/crid/1363107369023626624","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Cyclooctatetraene: A Bioactive Cubane Paradigm Complement"}]},{"@id":"https://cir.nii.ac.jp/crid/1363107369454830720","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Beyond C, H, O, and N! Analysis of the Elemental Composition of U.S. FDA Approved Drug Architectures"}]},{"@id":"https://cir.nii.ac.jp/crid/1363107369853134080","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Escape from Flatland: Increasing Saturation as an Approach to Improving Clinical Success"}]},{"@id":"https://cir.nii.ac.jp/crid/1363388843641420800","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Octacyclopropylcubane and Some of Its Isomers"}]},{"@id":"https://cir.nii.ac.jp/crid/1363388844692807552","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"The Lipophilic Bullet Hits the Targets: Medicinal Chemistry of Adamantane Derivatives"}]},{"@id":"https://cir.nii.ac.jp/crid/1363951794909894784","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Pseudotetrahedral Polyhalocubanes:  Synthesis, Structures, and Parity Violating Energy Differences"}]},{"@id":"https://cir.nii.ac.jp/crid/1364233270595923200","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Rings in Drugs"}]},{"@id":"https://cir.nii.ac.jp/crid/1364233270692723200","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"The cubane paradigm in bioactive molecule discovery: further scope, limitations and the cyclooctatetraene complement"}]},{"@id":"https://cir.nii.ac.jp/crid/1364233271020200320","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Click Chemistry: 1,2,3‐Triazoles as Pharmacophores"}]},{"@id":"https://cir.nii.ac.jp/crid/1390001204143978368","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Stereoisograms of Cubane Derivatives"},{"@value":"Seleted Paper : Stereoisograms of Cubane Derivatives"}]},{"@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/acs.orglett.0c01142"},{"@type":"KAKEN","@value":"PRODUCT-23744047"},{"@type":"KAKEN","@value":"PRODUCT-22829371"},{"@type":"OPENAIRE","@value":"doi_dedup___::18bf82ee47bf4106811c5672280cb45a"},{"@type":"CROSSREF","@value":"10.1021/acs.orglett.1c03144_references_DOI_EPPdvBO2tPyewXO3cvErSeGK9IR"},{"@type":"CROSSREF","@value":"10.1021/acs.orglett.2c03659_references_DOI_EPPdvBO2tPyewXO3cvErSeGK9IR"},{"@type":"CROSSREF","@value":"10.1002/ejoc.202200567_references_DOI_EPPdvBO2tPyewXO3cvErSeGK9IR"},{"@type":"CROSSREF","@value":"10.1246/cl.230101_references_DOI_EPPdvBO2tPyewXO3cvErSeGK9IR"},{"@type":"CROSSREF","@value":"10.1021/acs.orglett.3c04019_references_DOI_EPPdvBO2tPyewXO3cvErSeGK9IR"},{"@type":"CROSSREF","@value":"10.1002/ejoc.202300891_references_DOI_EPPdvBO2tPyewXO3cvErSeGK9IR"},{"@type":"CROSSREF","@value":"10.5059/yukigoseikyokaishi.83.46_references_DOI_EPPdvBO2tPyewXO3cvErSeGK9IR"},{"@type":"CROSSREF","@value":"10.1002/ijch.202100013_references_DOI_EPPdvBO2tPyewXO3cvErSeGK9IR"},{"@type":"CROSSREF","@value":"10.1055/a-2403-1860_references_DOI_EPPdvBO2tPyewXO3cvErSeGK9IR"},{"@type":"CROSSREF","@value":"10.1246/cl.220197_references_DOI_EPPdvBO2tPyewXO3cvErSeGK9IR"},{"@type":"CROSSREF","@value":"10.1055/a-2124-3823_references_DOI_EPPdvBO2tPyewXO3cvErSeGK9IR"}]}