Zobrazeno 1 - 10 of 10 pro vyhledávání: '"Michèle Janssen"'
1
Tetraphenol-based diphosphite ligands: synthesis, characterization, and application in the rhodium-catalyzed hydroformylation of octenes
Autor: Dieter Vogt, Dieter Hess, Bart Hamers, Andrea Christiansen, Laura Bini, Robert Franke, Christian Müller, Michèle Janssen
Publikováno v: Tetrahedron Letters, 51(15), 1971-1975. Elsevier
A new class of diphosphites is described, based on a tetraphenol backbone. Ligands TP1–TP5 were synthesized and fully characterized and their application in the hydroformylation of octenes was investigated. Ligand TP3, bearing a 1-naphthoxy substit
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a401828d4d1d4b9a073911bcac746d4
https://doi.org/10.1016/j.tetlet.2010.02.035
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2
Continuous rhodium-catalyzed hydroformylation of 1-octene with polyhedral oligomeric silsesquioxanes (POSS) enlarged triphenylphosphine
Autor: Christian Müller, Mcc Michèle Janssen, Jbm Jos Wilting, Dieter Vogt
Publikováno v: Angewandte Chemie-International Edition, 49(42), 7738-7741. Wiley
Angewandte Chemie, 122(42), 7904-7907. Wiley-VCH Verlag
Go with the flow: Homogeneous catalyst recycling can be applied to the production of aldehydes in a continuous flow nanofiltration reactor (see picture) that can operate for an unprecedented period of up to two weeks without showing typical deactivat
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f1ecc7a94924d9440db0c9b6aefac22
https://research.tue.nl/en/publications/1a6501fc-ab1a-45fc-b237-060df91103fe
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3
Molecular weight enlargement - a molecular approach to continuous homogeneous catalysis
Autor: Mcc Michèle Janssen, Dieter Vogt, Christian Müller
Publikováno v: Dalton Transactions, 39(36), 8403-8411. Royal Society of Chemistry
Molecular weight enlargement (MWE) is an attractive method for homogeneous catalyst recycling. Applications of MWE in combination with either catalyst precipitation or nanofiltration have demonstrated their great potential as a method for process int
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb201c86f52ef1cb399744ab122f5832
https://doi.org/10.1039/c0dt00175a
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4
‘Click’ Dendritic Phosphines: Design, Synthesis, Application in Suzuki Coupling, and Recycling by Nanofiltration
Autor: Dieter Vogt, Christian Müller, Michèle Janssen
Publikováno v: Advanced Synthesis & Catalysis, 351(3), 313-318. Wiley-VCH Verlag
A new synthetic route towards stable molecular-weight enlarged monodentate phosphine ligands via 'click' chemistry was developed. These ligands were applied in the Pd-catalyzed Suzuki-Miyaura coupling of aryl halides and phenyl boronic acid. The supp
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d50039d36edb83f195d9560995effcf9
https://doi.org/10.1002/adsc.200900058
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5
Binaphthol-based diphosphite ligands in asymmetric nickel-catalyzed hydrocyanation of styrene and 1,3-cyclohexadiene: Influence of steric properties
Autor: Christian Müller, Anthony L. Spek, Dieter Vogt, Mcc Michèle Janssen, Jbm Jos Wilting, Martin Lutz
Publikováno v: Wilting, J, Janssen, M H M, Muller, C J, Lutz, M, Spek, A L & Vogt, D 2007, ' Binaphthol-based diphosphite ligands in asymmetric nickel-catalyzed hydrocyanation of styrene and 1,3-cyclohexadiene: Influence of steric properties ', Advanced Synthesis and Catalysis, vol. 349, no. 3, pp. 350-356 . https://doi.org/10.1002/adsc.200600315
Advanced Synthesis & Catalysis, 349(3), 350-356. Wiley-VCH Verlag
Advanced Synthesis and Catalysis, 349(3), 350-356. Wiley-VCH Verlag
A series of chiral (R)-binaphthol-based di- phosphite ligands with different substituents was pre- pared and applied in the asymmetric nickel-catalyzed hydrocyanation of styrene and 1,3-cyclohexadiene to investigate the influence of their steric prop
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0b25f980eb1e2a04bd43b211d7f7a90
https://hdl.handle.net/1871/30952
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9
The enantioselective step in the nickel-catalyzed hydrocyanation of 1,3-cyclohexadiene
Autor: Dieter Vogt, Michèle Janssen, Jos Wilting, Christian Müller
Publikováno v: Wilting, J, Janssen, M H M, Muller, C J & Vogt, D 2006, ' The enantioselective step in the nickel-catalyzed hydrocyanation of 1,3-cyclohexadiene ', Journal of the American Chemical Society, vol. 128, no. 35, pp. 11374-5 . https://doi.org/10.1021/ja064378u
Journal of the American Chemical Society, 128(35), 11374-11375. American Chemical Society
Journal of the American Chemical Society, 128(35), 11374-5. American Chemical Society
On the basis of deuterium labeling experiments and an equal 1,2-/1,4-product distribution, the reductive elimination of the product has been established to be the enantioselective step in the nickel-catalyzed hydrocyanation of 1,3-cyclohexadiene. Thi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edca6a89b032a47abdde7f50bf5e60e9
https://hdl.handle.net/1871/27870
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10
Recent advances in the recycling of homogeneous catalysts using membrane separation
Autor: Mcc Michèle Janssen, Dieter Vogt, Christian Müller
Publikováno v: Green Chemistry, 13, 2247-2257. Royal Society of Chemistry
Membrane filtration is an attractive approach for soluble catalyst recycling. Applications of nanofiltration have demonstrated their great potential as a method for process intensification in enzyme, organo-, and homogeneous catalysis, both in labora
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83d5abadc55b6e0b822c23d3c5a6216d
https://doi.org/10.1039/c1gc15264e
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