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http://hdl.handle.net/2445/129449
Title: | Extending the substrate scope in the hydrogenation of unfunctionalized tetrasubstituted olefins with Ir-P stereogenic aminophosphine-oxazoline catalysts |
Author: | Biosca, Maria Salomó i Prat, Ernest Cruz Sánchez, Pol de la Riera i Escalé, Antoni Verdaguer i Espaulella, Xavier Pàmies, Oscar Diéguez, Montserrat |
Keywords: | Hidrogenació Catàlisi Lligands (Bioquímica) Hydrogenation Catalysis Ligands (Biochemistry) |
Issue Date: | 16-Jan-2019 |
Publisher: | American Chemical Society |
Abstract: | Air stable and readily available Ir-catalyst precursors modified with MaxPHOX-type ligands have been successfully applied in the challenging asymmetric hydrogenation of tetrasubstituted olefins under mild reaction conditions. Gratifyingly, these catalyst precursors are not only able to efficiently hydrogenate a range of indene derivatives (ee's up to 96%) but also 1,2-dihydro-napthalene derivatives and acyclic olefins (ee's up to 99%), which both constitute the most challenging substrates for this transformation. |
Note: | Versió postprint del document publicat a: https://doi.org/10.1021/acs.orglett.8b04084 |
It is part of: | Organic Letters, 2019, vol. 21, num. 3, p. 807-811 |
URI: | http://hdl.handle.net/2445/129449 |
Related resource: | https://doi.org/10.1021/acs.orglett.8b04084 |
ISSN: | 1523-7060 |
Appears in Collections: | Articles publicats en revistes (Química Inorgànica i Orgànica) |
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686530.pdf | 219.51 kB | Adobe PDF | View/Open |
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