Author, as appears in the article.: Pàmies O, Magre M, Diéguez M
Department: Química Física i Inorgànica Química Física i Inorgànica
URV's Author/s: Diéguez Fernández, Montserrat / Pamies Ollé, Oscar
Keywords: P,s ligands P,n ligands Ligand design Iridium Hydrogenation Asymmetric hydrogenation p,s ligands p,n ligands iridium hydrogenation
Abstract: Asymmetric hydrogenation is one of the most efficient and atom-economical tools to prepare chiral molecules. However, the enantiodiscrimination of simple, minimally functionalized olefins is still challenging and requires more sophisticated ligand design. Herein, we discuss our progress in the successful development of ligand design for the iridium-catalyzed asymmetric hydrogenation of minimally functionalized olefins
Thematic Areas: Medicine (miscellaneous) Materials chemistry General chemistry General chemical engineering Engenharias ii Ciência de alimentos Chemistry, multidisciplinary Chemistry (miscellaneous) Chemistry (all) Chemical engineering (miscellaneous) Chemical engineering (all) Biochemistry (medical) Biochemistry
ISSN: 15278999
Author's mail: oscar.pamies@urv.cat montserrat.dieguez@urv.cat
Author identifier: 0000-0002-2352-8508 0000-0002-8450-0656
Record's date: 2024-09-07
Licence document URL: https://repositori.urv.cat/ca/proteccio-de-dades/
Papper original source: Chemical Record. 16 (3): 1578-1590
APA: Pàmies O, Magre M, Diéguez M (2016). Extending the Substrate Scope for the Asymmetric Iridium-Catalyzed Hydrogenation of Minimally Functionalized Olefins by Using Biaryl Phosphite-Based Modular Ligand Libraries. Chemical Record, 16(3), 1578-1590. DOI: 10.1002/tcr.201600024
Entity: Universitat Rovira i Virgili
Journal publication year: 2016
Publication Type: Journal Publications
Repositori URV