Pseudo-multicomponent 1,3-dipolar cycloaddition involving metal-free generation of unactivated azomethine ylides
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http://hdl.handle.net/10045/131882
Títol: | Pseudo-multicomponent 1,3-dipolar cycloaddition involving metal-free generation of unactivated azomethine ylides |
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Autors: | Belabbes, Asmaa | Retamosa, Maria de Gracia | Foubelo, Francisco | Sirvent, Ana | Nájera, Carmen | Yus, Miguel | Sansano, Jose M. |
Grups d'investigació o GITE: | Síntesis Asimétrica (SINTAS) |
Centre, Departament o Servei: | Universidad de Alicante. Departamento de Química Orgánica | Universidad de Alicante. Instituto Universitario de Síntesis Orgánica |
Paraules clau: | Pseudo-multicomponent | 1,3-dipolar cycloaddition | Metal-free generation | Unactivated azomethine ylides |
Data de publicació: | 27-de gener-2023 |
Editor: | Royal Society of Chemistry |
Citació bibliogràfica: | Organic & Biomolecular Chemistry. 2023, 21: 1927-1936. https://doi.org/10.1039/D3OB00023K |
Resum: | The pseudo-multicomponent reaction between propargyl amine, an aldehyde and an electron-deficient alkene is described. The C–H activation takes place thermally and allows the obtaining of cycloadducts in very good yields with high diastereoselectivities. The relative configuration is determined by X-ray diffraction analysis of the chiral molecule, obtained as a single diastereoisomer, using a chiral maleimide. A brief study of the stability of the possible ylides involved in the process is also mentioned, confirming the high diastereoselectivity observed. The high functional group density of these cycloadducts permits the synthesis of complex heterocycles. After allylation or propargylation of the pyrrolidine nitrogen atom, RCM-DA cycloaddition or cyclotrimerization with an alkyne is studied, respectively. In this last example, the resulting tetracyclic structures are of potential interest as drugs for the treatment of cystic fibrosis. |
Patrocinadors: | We gratefully acknowledge financial support from the Spanish Ministerio de Ciencia, Innovación y Universidades (project RED2018-102387-T) the Spanish Ministerio de Economía, Industria y Competitividad, Agencia Estatal de Investigación (AEI) and Fondo Europeo de Desarrollo Regional (FEDER, EU) (projects CTQ2017-82935-P and PID2019-107268GB-I00), the Generalitat Valenciana (IDIFEDER/2021/013, GVA-COVID19/2021/079 and CIDEGENT/2020/058), Medalchemy S.L. (Medalchemy-18T) and the University of Alicante (VIGROB-068, UAUSTI21-05). |
URI: | http://hdl.handle.net/10045/131882 |
ISSN: | 1477-0520 (Print) | 1477-0539 (Online) |
DOI: | 10.1039/D3OB00023K |
Idioma: | eng |
Tipus: | info:eu-repo/semantics/article |
Drets: | © Royal Society of Chemistry 2023 |
Revisió científica: | si |
Versió de l'editor: | https://doi.org/10.1039/D3OB00023K |
Apareix a la col·lecció: | INV - SINTAS - Artículos de Revistas |
Arxius per aquest ítem:
Arxiu | Descripció | Tamany | Format | |
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Belabbes_etal_2023_OrgBiomolChem_accepted.pdf | Accepted Manuscript (acceso abierto) | 1,13 MB | Adobe PDF | Obrir Vista prèvia |
Belabbes_etal_2023_OrgBiomolChem_final.pdf | Versión final (acceso restringido) | 623,65 kB | Adobe PDF | Obrir Sol·licitar una còpia |
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