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Källström, Klas
Publikasjoner (5 av 5) Visa alla publikasjoner
Källström, K. & Andersson, P. (2006). Asymmetric hydrogenation of tri-substituted alkenes with Ir-NHC-thiazole complexes. Tetrahedron Letters, 47(42), 7477-7480
Åpne denne publikasjonen i ny fane eller vindu >>Asymmetric hydrogenation of tri-substituted alkenes with Ir-NHC-thiazole complexes
2006 (engelsk)Inngår i: Tetrahedron Letters, ISSN 0040-4039, E-ISSN 1359-8562, Vol. 47, nr 42, s. 7477-7480Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

An efficient chiral N-heterocyclic carbene ligand for the Ir-catalyzed asymmetric hydrogenation of largely unfunctionalized tri-substituted olefins has been developed. The Ir-NHC-thiazole catalyst is able to reduce a large variety of substrates with excellent conversions and good enantioselectivities with ee's ranging from 34% to 90%, depending on the geometry around the double bond of the substrates.

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urn:nbn:se:uu:diva-84297 (URN)10.1016/j.tetlet.2006.08.039 (DOI)000241063900018 ()
Tilgjengelig fra: 2006-11-14 Laget: 2006-11-14 Sist oppdatert: 2017-12-14bibliografisk kontrollert
Källström, K., Munslow, I. & Andersson, P. (2006). Ir-Catalysed Asymmetric Hydrogenation: Ligands, Substrates and Mechanism. Chem. Eur. J. (12), 3194-3200
Åpne denne publikasjonen i ny fane eller vindu >>Ir-Catalysed Asymmetric Hydrogenation: Ligands, Substrates and Mechanism
2006 (engelsk)Inngår i: Chem. Eur. J., nr 12, s. 3194-3200Artikkel i tidsskrift (Fagfellevurdert) Published
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urn:nbn:se:uu:diva-84301 (URN)doi:10.1002/chem.200500755 (DOI)
Tilgjengelig fra: 2006-11-14 Laget: 2006-11-14 Sist oppdatert: 2011-01-11
Hedberg, C., Källström, K., Arvidsson, P., Brandt, P. & Andersson, P. (2005). Mechanistic Insights into the Phosphine-Free RuCp*-Diamine-Catalyzed Hydrogenation of Aryl Ketones: Experimental and Theoretical Evidence for an Alcohol-Mediated Dihydrogen Activation. J. Am. Chem. Soc. (127), 15083-15090
Åpne denne publikasjonen i ny fane eller vindu >>Mechanistic Insights into the Phosphine-Free RuCp*-Diamine-Catalyzed Hydrogenation of Aryl Ketones: Experimental and Theoretical Evidence for an Alcohol-Mediated Dihydrogen Activation
Vise andre…
2005 (engelsk)Inngår i: J. Am. Chem. Soc., nr 127, s. 15083-15090Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract
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urn:nbn:se:uu:diva-84289 (URN)doi:10.1021/ja051920Q (DOI)
Tilgjengelig fra: 2006-11-14 Laget: 2006-11-14 Sist oppdatert: 2016-08-17
Källström, K., Hedberg, C., Brandt, P., Bayer, A. & Andersson, P. G. (2004). Rationally Designed Ligands for Asymmetric Iridium-Catalyzed Hydrogenation of Olefins. Journal of the American Chemical Society, 126(44), 14308-14309
Åpne denne publikasjonen i ny fane eller vindu >>Rationally Designed Ligands for Asymmetric Iridium-Catalyzed Hydrogenation of Olefins
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2004 (engelsk)Inngår i: Journal of the American Chemical Society, ISSN 0002-7863, E-ISSN 1520-5126, Vol. 126, nr 44, s. 14308-14309Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

A new class of chiral N,P-ligands for the Ir-catalyzed asymmetric hydrogenation of aryl alkenes has been developed. These new ligands proved to be highly efficient and tolerates a broad range of substrates. The enantiomeric excesses are in the range of the best ever reported. The results can be rationalized with the proposed selectivity model.

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American Chemical Society (ACS), 2004
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urn:nbn:se:uu:diva-92879 (URN)10.1021/ja0464241 (DOI)000224964500003 ()2-s2.0-7744246546 (Scopus ID)
Tilgjengelig fra: 2005-04-07 Laget: 2005-04-07 Sist oppdatert: 2025-04-01bibliografisk kontrollert
Ekegren, J., Roth, P., Källström, K., Tarnai, T. & Andersson, P. (2003). Synthesis and evaluation of N,S-compounds as chiral ligands for transfer hydrogenation of acetophenone. Org. Biomol. Chem (1), 358-366
Åpne denne publikasjonen i ny fane eller vindu >>Synthesis and evaluation of N,S-compounds as chiral ligands for transfer hydrogenation of acetophenone
Vise andre…
2003 (engelsk)Inngår i: Org. Biomol. Chem, nr 1, s. 358-366Artikkel i tidsskrift (Fagfellevurdert) Published
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urn:nbn:se:uu:diva-84390 (URN)doi:10.1039/b208907f (DOI)
Tilgjengelig fra: 2006-11-15 Laget: 2006-11-15 Sist oppdatert: 2011-01-13
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