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| dc.contributor.author | Virumbrales Ortiz, Cintia | |
| dc.contributor.author | Mahmoud Abd El Aleem Ali, Elremaily | |
| dc.contributor.author | Suarez Pantiga, Samuel | |
| dc.contributor.author | Fernández Rodríguez, Manuel A. | |
| dc.contributor.author | Rodríguez, Félix | |
| dc.contributor.author | Sanz Díez, Roberto | |
| dc.date.accessioned | 2023-02-07T08:26:25Z | |
| dc.date.available | 2023-02-07T08:26:25Z | |
| dc.date.issued | 2022-10 | |
| dc.identifier.issn | 1523-7060 | |
| dc.identifier.uri | http://hdl.handle.net/10259/7405 | |
| dc.description.abstract | A gold(I)-catalyzed cascade reaction for the stereoselective synthesis of sulfur- or selenium-containing indeno[1,2-b]chromene derivatives from o-(alkynyl)styrenes substituted at the triple bond with a thio- or seleno-aryl group is described. The reaction involves a double cyclization process through a proposed key gold−cyclopropyl carbene intermediate that evolves by the intramolecular addition of an aromatic to the cyclopropane ring, affording polycyclic structures. The enantioselective version was studied using gold(I) complexes bearing chiral ligands. | en |
| dc.description.sponsorship | We gratefully acknowledge MICINN (PID2020-115789GBC21), “NextGenerationEU/PRTR” (PDC2021-120825-C21), Junta de Castilla y León, and FEDER (BU049P20) for financial support. The project leading to these results also received funding from the “la Caixa” Foundation, under Agreement LCF/PR/PR18/51130007 (CAIXA-UBU001). C.V. and S.S.-P. thank Junta de Castilla y León (Consejería de Educación) and Fondo Social Europeo for postdoctoral contracts. | en |
| dc.format.mimetype | application/pdf | |
| dc.language.iso | eng | es |
| dc.publisher | American Chemical Society | en |
| dc.relation.ispartof | Organic Letters. 2022, V. 24, n. 43, p. 8077-8082 | es |
| dc.rights | Atribución 4.0 Internacional | * |
| dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | * |
| dc.subject | Carbene compounds | en |
| dc.subject | Gold | en |
| dc.subject | Hydrocarbons | en |
| dc.subject | Molecular structure | en |
| dc.subject | Reaction products | en |
| dc.subject.other | Química orgánica | es |
| dc.subject.other | Chemistry, Organic | en |
| dc.title | Gold(I) Catalysis Applied to the Stereoselective Synthesis of Indeno[2,1-b]thiochromene Derivatives and Seleno Analogues | en |
| dc.type | info:eu-repo/semantics/article | es |
| dc.rights.accessRights | info:eu-repo/semantics/openAccess | es |
| dc.relation.publisherversion | https://doi.org/10.1021/acs.orglett.2c03411 | es |
| dc.identifier.doi | 10.1021/acs.orglett.2c03411 | |
| dc.relation.projectID | info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2020-115789GB-C21/ES/ESTRATEGIAS SINTETICAS SOSTENIBLES PARA LA TRANSFORMACION DIRECTA DE NITROCOMPUESTOS Y DESARROLLO DE NUEVAS REACCIONES CATALIZADAS POR ORO/ | es |
| dc.relation.projectID | info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PDC2021-120825-C21/ES/Valorización de productos de la biomasa por catálisis con complejos de dioxomolibdeno/ | es |
| dc.relation.projectID | info:eu-repo/grantAgreement/Junta de Castilla y León//BU049P20//Estrategias sintéticas sostenibles para la halogenación directa de nitrocompuestos y la preparación de electrolitos orgánicos para baterías de flujo redox/ | es |
| dc.relation.projectID | info:eu-repo/grantAgreement/Fundación Bancaria Caixa d'Estalvis i Pensions de Barcelona//LCF%2FPR%2FPR18%2F51130007/Fluoración Directa de Nitrocompuestos y Sales de Heteroaril Fosfonio: Síntesis de Fluorocompuestos/FluNitroPhos/ | es |
| dc.identifier.essn | 1523-7052 | |
| dc.journal.title | Organic Letters | en |
| dc.volume.number | 24 | es |
| dc.issue.number | 43 | es |
| dc.page.initial | 8077 | es |
| dc.page.final | 8082 | es |
| dc.type.hasVersion | info:eu-repo/semantics/publishedVersion | es |
