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Transition metal-free cyclobutene rearrangement in fused naphthalen-1-ones: controlled access to functionalized quinones

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dc.contributor.authorLuna Costales, Amparo
dc.contributor.authorHerrera García, Fernando
dc.contributor.authorAlmendros Requena, Pedro
dc.contributor.authorFernández López, Israel
dc.date.accessioned2025-01-10T18:57:47Z
dc.date.available2025-01-10T18:57:47Z
dc.date.issued2019-12-19
dc.description.abstractThe controlled synthesis of 1,4-naphthoquinones and tetraphene7,12-diones, which bear the ABCD-ring of landomycins, has been accomplished directly through oxidative rearrangement of common stable precursors, namely, previously non-isolable cyclobuta[a]naphthalen4(2H)-ones.
dc.description.departmentDepto. de Química Orgánica
dc.description.facultyFac. de Ciencias Químicas
dc.description.refereedTRUE
dc.description.sponsorshipMinisterio de Ciencia e Innovación (España)
dc.description.sponsorshipEuropean Commission
dc.description.statuspub
dc.identifier.citationHerrera Fernando, Luna Amparo, Fernández Israel, Almendros Pedro. Transition metal-free cyclobutene rearrangement in fused naphthalen-1-ones: controlled access to functionalized quinones. Chem. Commun., 2020, 56 (8), 1290-1293
dc.identifier.doi10.1039/C9CC08628E
dc.identifier.essn1364-548X
dc.identifier.issn1359-7345
dc.identifier.officialurlhttps://pubs.rsc.org/en/content/articlelanding/2020/cc/c9cc08628e
dc.identifier.pmid31904044
dc.identifier.relatedurlhttps://digital.csic.es/handle/10261/209781
dc.identifier.relatedurlhttps://pubmed.ncbi.nlm.nih.gov/31904044/
dc.identifier.urihttps://hdl.handle.net/20.500.14352/113815
dc.issue.number8
dc.journal.titleChemical Communications
dc.language.isoeng
dc.page.final1293
dc.page.initial1290
dc.publisherRoyal Society of Chemistry
dc.relation.projectIDPGC2018-095025-B-I00
dc.relation.projectIDCTQ2016-78205-P
dc.relation.projectIDCTQ2016-81797-REDC
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.cdu547
dc.subject.keywordquinone
dc.subject.keyword1,4-naphthoquinones
dc.subject.keywordallenynols
dc.subject.ucmQuímica orgánica (Química)
dc.subject.unesco2306 Química Orgánica
dc.subject.unesco2306.10 Compuestos Heterocíclicos
dc.titleTransition metal-free cyclobutene rearrangement in fused naphthalen-1-ones: controlled access to functionalized quinones
dc.typejournal article
dc.type.hasVersionAM
dc.volume.number56
dspace.entity.typePublication
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relation.isAuthorOfPublication75f8e5ee-a396-49cb-bcf1-dbd26713962b
relation.isAuthorOfPublicationee8363b4-4019-453d-abd3-6258ecc4299f
relation.isAuthorOfPublicationb2a789aa-d9bf-4564-b0e2-35b8de8d6d06
relation.isAuthorOfPublication.latestForDiscovery14581fe9-97b8-4d33-920f-23f4778c49f7

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