Repositori institucional URV
| Autor/es de la URV: | Biosca Brull, Maria / De La Cruz Sánchez Badia, Pol / Diéguez Fernández, Montserrat / Faiges Marcos, Jorge / Margalef Pallarès, Jèssica / Pamies Ollé, Oscar |
| Autor según el artículo: | Margalef, J; Biosca, M; Sánchez, PD; Faiges, J; Pàmies, O; Diéguez, M |
| Direcció de correo del autor: | maria.biosca@urv.cat pol.delacruzsanchez@estudiants.urv.cat pol.delacruzsanchez@estudiants.urv.cat jorge.faiges@estudiants.urv.cat oscar.pamies@urv.cat oscar.pamies@urv.cat montserrat.dieguez@urv.cat montserrat.dieguez@urv.cat |
| Identificador del autor: | 0000-0002-9116-6318 0000-0002-2352-8508 0000-0002-2352-8508 0000-0002-8450-0656 0000-0002-8450-0656 |
| Año de publicación de la revista: | 2021-11-01 |
| Tipo de publicación: | Journal Publications |
| Referencia de l'ítem segons les normes APA: | Margalef, J; Biosca, M; Sánchez, PD; Faiges, J; Pàmies, O; Diéguez, M (2021). Evolution in heterodonor P-N, P-S and P-O chiral ligands for preparing efficient catalysts for asymmetric catalysis. From design to applications. COORDINATION CHEMISTRY REVIEWS, 446(), 214120-. DOI: 10.1016/j.ccr.2021.214120 |
| Referencia al articulo segun fuente origial: | COORDINATION CHEMISTRY REVIEWS. 446 214120- |
| Resumen: | The success of phosphine-oxazoline ligands (PHOX) inspired the progress in P-oxazoline ligand families by modifying either the ligand backbone, the electronic and/or steric properties of the phosphine group or by exchanging the phosphine to a phosphinite or a phosphite group. In this respect, the structures of chiral P-oxazoline ligands have become more diverse and new families of very efficient ligands have emerged, which have improved catalytic performance in some asymmetric transformations, with an increased versatility, both in the range of reactions and in the range of substrates/reagents. In addition, most of ligands are synthesized from easily accessible chiral amino alcohols, maintaining the short and efficient synthetic route developed for PHOX ligands. New ligands have been developed by replacing the oxazoline functionality with several other N-donor groups, e.g. imidazole, thiazole, oxazole, pyridine, etc., and O- and S-groups. This review offers a critical overview of the utility of these most successful bidentate heterodonor P-N, P-O and P-S ligand families applied in metal-mediated processes. We illustrate how, through proper ligand design, these heterodonor bidentate ligand families can be an excellent source of ligands, with superior catalytic performance in many asymmetric reactions than the best C-2-symmetric N,N and P,P-ligands reported so far. (C) 2021 The Authors. Published by Elsevier B.V. |
| DOI del artículo: | 10.1016/j.ccr.2021.214120 |
| Enlace a la fuente original: | https://www.sciencedirect.com/science/article/pii/S0010854521003945 |
| Versión del articulo depositado: | info:eu-repo/semantics/publishedVersion |
| Acceso a la licencia de uso: | https://creativecommons.org/licenses/by/3.0/es/ |
| Departamento: | Química Física i Inorgànica |
| URL Documento de licencia: | https://repositori.urv.cat/ca/proteccio-de-dades/ |
| Áreas temáticas: | Physical and theoretical chemistry Materials chemistry Inorganic chemistry General chemistry Chemistry, inorganic & nuclear Chemistry (miscellaneous) Chemistry (all) Biotecnología Astronomia / física |
| Palabras clave: | Transition-metal-complexes Selective 1,1-binaphthyl synthesis Phosphorus-containing oxazoline Phosphite-oxazoline ligands P-s ligands P-o ligands P-n ligands Minimally functionalized olefins Ligand design Enantioselective total-synthesis Diastereoselective mannich reaction Atropisomeric phosphinamine ligand Asymmetric catalysis Alpha,beta-unsaturated carboxylic-acids Allylic substitution-reactions |
| Entidad: | Universitat Rovira i Virgili |
| Fecha de alta del registro: | 2026-05-09 |
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