Por favor, use este identificador para citar o enlazar este ítem:
https://hdl.handle.net/10495/37988
Registro completo de metadatos
Campo DC | Valor | Lengua/Idioma |
---|---|---|
dc.contributor.author | Prieto Mesa, Ana María | - |
dc.contributor.author | Otálvaro Tamayo, Felipe | - |
dc.contributor.author | Paetz, Christian | - |
dc.contributor.author | Schneider, Bernd | - |
dc.date.accessioned | 2024-02-02T19:58:03Z | - |
dc.date.available | 2024-02-02T19:58:03Z | - |
dc.date.issued | 2024 | - |
dc.identifier.citation | Prieto A, Paetz C, Schneider B, Otálvaro F. Synthesis of 5-phenyl-1,8-naphthalic anhydrides: An exercise in acenaphthene chemistry. Tetrahedron Lett [Internet]. 2024;135:154907. Disponible en: https://www.sciencedirect.com/science/article/pii/S0040403924000017 | spa |
dc.identifier.issn | 0040-4039 | - |
dc.identifier.uri | https://hdl.handle.net/10495/37988 | - |
dc.description.abstract | ABSTRACT: The synthesis of phenylnaphthalic anhydrides, including substitution patterns typically found in the Haemodoraceae and Pontederiacea family of plants, was explored using Suzuki and Ullmann-type aromatic substitutions on acenaphthene. Synthetic challenges were surmounted by tactical changes to determine the order of events. | spa |
dc.format.extent | 4 | spa |
dc.format.mimetype | application/pdf | spa |
dc.language.iso | eng | spa |
dc.publisher | Elsevier | spa |
dc.type.hasversion | info:eu-repo/semantics/publishedVersion | spa |
dc.rights | info:eu-repo/semantics/openAccess | spa |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/2.5/co/ | * |
dc.title | Synthesis of 5-phenyl-1,8-naphthalic anhydrides: An exercise in acenaphthene chemistry | spa |
dc.type | info:eu-repo/semantics/article | spa |
dc.publisher.group | Síntesis y Biosíntesis de Metabolitos Naturales | spa |
dc.identifier.doi | 10.1016/j.tetlet.2024.154907 | - |
oaire.version | http://purl.org/coar/version/c_970fb48d4fbd8a85 | spa |
dc.rights.accessrights | http://purl.org/coar/access_right/c_abf2 | spa |
oaire.citationtitle | Tetrahedron Letters | spa |
oaire.citationstartpage | 1 | spa |
oaire.citationendpage | 4 | spa |
oaire.citationvolume | 135 | spa |
dc.rights.creativecommons | https://creativecommons.org/licenses/by-nc-nd/4.0/ | spa |
oaire.fundername | Universidad de Antioquia. Vicerrectoría de investigación. Comité para el Desarrollo de la Investigación - CODI | spa |
oaire.fundername | Max Planck Institute for Chemical Ecology | spa |
dc.publisher.place | Oxford, Inglaterra | spa |
dc.type.coar | http://purl.org/coar/resource_type/c_2df8fbb1 | spa |
dc.type.redcol | https://purl.org/redcol/resource_type/ART | spa |
dc.type.local | Artículo de investigación | spa |
dc.subject.proposal | Phenylnaphthalic anhydrides | spa |
dc.subject.proposal | Acenaphthene chemistry | spa |
dc.subject.proposal | Suzuki coupling | spa |
dc.subject.proposal | Ullman-type substitution | spa |
dc.description.researchgroupid | COL0069689 | spa |
oaire.awardnumber | ES84220018 | spa |
dc.relation.ispartofjournalabbrev | Tetrahedron. Lett. | spa |
oaire.funderidentifier.ror | RoR:03bp5hc83 | - |
oaire.funderidentifier.ror | RoR:02ks53214 | - |
Aparece en las colecciones: | Artículos de Revista en Ciencias Exactas y Naturales |
Ficheros en este ítem:
Fichero | Descripción | Tamaño | Formato | |
---|---|---|---|---|
PrietoAna_2024_Synthesis5Phenyl1.pdf | Artículo de investigación | 577.71 kB | Adobe PDF | Visualizar/Abrir |
Este ítem está sujeto a una licencia Creative Commons Licencia Creative Commons