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Rationally Designed Ligands for Asymmetric Iridium-Catalyzed Hydrogenation of Olefins
Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Chemistry.
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2004 In: Journal of the American Chemical Society, ISSN 0002-7863, Vol. 126, no 44, 14308-14309 p.Article in journal (Refereed) Published
Place, publisher, year, edition, pages
2004. Vol. 126, no 44, 14308-14309 p.
URN: urn:nbn:se:uu:diva-92879OAI: oai:DiVA.org:uu-92879DiVA: diva2:166190
Available from: 2005-04-07 Created: 2005-04-07 Last updated: 2016-08-17Bibliographically approved
In thesis
1. Design, Synthesis, Mechanistic Rationalization and Application of Asymmetric Transition-Metal Catalysts
Open this publication in new window or tab >>Design, Synthesis, Mechanistic Rationalization and Application of Asymmetric Transition-Metal Catalysts
2005 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

This thesis describes mechanistic studies, rational ligand design, and synthesis of asymmetric transition metal catalysts. The topics addressed concerned [Papers I-VII]:

[I] The asymmetric addition of diethyl zinc to N-(diphenylphosphinoyl)benzalimine catalyzed by bicyclic 2-azanorbornyl-3-methanols was studied. An efficient route to both diastereomers of new bicyclic 2-azanorbornyl-3-methanols with an additional chiral center was developed, in the best case 97% ee was obtained with these ligands. The experimental results were rationalized by a computational DFT-study.

[II] An aza-Diels-Alder reaction of cyclopentadiene with chiral heterocyclic imines derived from (S)-1-phenylethylamine and different heteroaromatic aldehydes was developed. The cycloaddition proved to be highly diastereoselective and offers a very rapid access to possible biologically active compounds and interesting precursors for chiral (P,N)-ligands.

[III] A convenient and high-yielding method for the preparation of (R)-tolterodine, utilizing a catalytic asymmetric Me-CBS reduction was developed. Highly enantio-enriched (R)-6-methyl-4-phenyl-3,4-dihydrochromen-2-one (94% ee) was recrystallized to yield practically enantiopure material (ee >99%) and converted to (R)-tolterodine in a four-step procedure.

[IV] The reaction mechanism of the iridium-phosphanooxazoline-catalyzed hydrogenation of unfunctionalized olefins has been studied by means of DFT-calculations (B3LYP) and kinetic experiments. The calculations suggest that the reaction involves an unexpected IrIII-IrV catalytic cycle facilitated by coordination of a second equivalent of dihydrogen. On the basis of the proposed catalytic cycle, calculations were performed on a full system with 88 atoms. These calculations were also used to explain the enantioselectivity displayed by the catalyst.

[V and VI] A new class of chiral (P,N)-ligands for the Ir-catalyzed asymmetric hydrogenation of aryl alkenes was developed. These new ligands proved to be highly efficient and tolerate a broad range of substrates. The enantiomeric excesses are, so far, the best reported and can be rationalized using the proposed selectivity model.

[VII] The complex formed between the quincorine-amine, containing both a primary and a quinuclidine amino function, and [Cp*RuCl]4 catalyzes the hydrogenation of aromatic and aliphatic ketones in up to 90% ee approx. 24-times faster than previously reported Ru-diamine complexes. The reason for the lower but opposite stereoselectivity seen with the quincoridine-amine, as compared to the quincorine-amine, was rationalized by a kinetic and computational study of the mechanism. The theoretical calculations also revealed a significantly lower activation barrier for the alcohol mediated split of dihydrogen, as compared to the non-alchol mediated process. A finding of importance also for the diphosphine/diamine mediated enantioselective hydrogenation of ketones.

Place, publisher, year, edition, pages
Uppsala: Acta Universitatis Upsaliensis, 2005. 81 p.
Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology, ISSN 1651-6214 ; 36
Organic chemistry, asymmetric catalysis, homogeneous hydrogenation, iridium, ruthenium, ligand design, mechanistic studies, kinetics, tolterodine, Organisk kemi
National Category
Organic Chemistry
urn:nbn:se:uu:diva-5740 (URN)91-554-6209-X (ISBN)
Public defence
2005-04-28, B22, BMC, Husargatan 3, Uppsala, 10:15
Available from: 2005-04-07 Created: 2005-04-07Bibliographically approved

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