Zobrazeno 1 - 9 of 9 pro vyhledávání: '"Mie Højer Larsen"'
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Core carbo ‐mer of an Extended Tetrathiafulvalene: Redox‐Controlled Reversible Conversion to a carbo ‐Benzenic Dication
Autor: Carine Duhayon, Ole Hammerich, Dymytrii Listunov, Albert Poater, Gabriel Ramos-Ortiz, Valérie Maraval, Mie Højer Larsen, Irving Caballero-Quintana, Mogens Nielsen, José-Luis Maldonado, Cécile Barthes, Remi Chauvin
Publikováno v: Chemistry-A European Journal
Chemistry-A European Journal, Wiley-VCH Verlag, 2020, 26 (47), pp.10707-10711. ⟨10.1002/chem.202001700⟩
International audience; Carbo -benzene is an aromatic molecule devised by inserting C 2 units within each C-C bond of the benzene molecule. By integrating the corresponding carbo -quinoid core as bridging unit in a p -extended tetrathiafulvalene (exT
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7c1288ac1d3dfd27dc2a56141bc3037
https://doi.org/10.1002/chem.202001700
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2
Gold catalysis: Experimental mechanistic insights into the anellation of phenols with 1,3-dienes
Autor: Kumara Swamy Nalivela, Sarah Bay, Alexandra Englert, A. Stephen K. Hashmi, Mie Højer Larsen
Publikováno v: Journal of Organometallic Chemistry. 795:58-62
An intermediate of the anellation reaction of phenols and 1,3-dienes could be detected, isolated and characterized as the hydroarylation product. The other conceivable intermediate, the hydroaryloxylation product, was prepared via Pd-catalysis and co
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::780252201fafb1a9c0c7f0552af8dc7c
https://doi.org/10.1016/j.jorganchem.2015.05.034
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3
Gold-catalyzed nucleophilic tandem cyclizations of tetraethynylethene derivatives
Autor: A. Stephen K. Hashmi, Marcel Wieteck, Matthias Rudolph, Mie Højer Larsen, Johannes Schädlich
Publikováno v: Tetrahedron. 71:5858-5865
Symmetric and non-symmetric tetraethynylethene derivatives possessing nucleophilic groups were synthesized and subjected to gold catalysts. By a fourfold nucleophilic tandem cyclization extended π-systems like carbazolocarbazoles are accessible in h
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2d04d2475a57623a6ed04b040a4d34f9
https://doi.org/10.1016/j.tet.2015.06.011
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4
The Gilded Edge in Acetylenic Scaffolding II: A Computational Study of the Transmetalation Processes Involved in Palladium-Catalyzed Cross-Couplings of Gold(I) Acetylides
Autor: Mogens Brøndsted Nielsen, Mie Højer Larsen
Publikováno v: Organometallics. 34:3678-3685
The palladium-catalyzed cross-coupling reaction between phosphine-gold(I) acetylides and aryl iodides has recently proven as a convenient alternative to the standard Sonogashira reaction, which instead employs terminal alkynes as substrates. This alt
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::35437856f3296b6194a866097f42484e
https://doi.org/10.1021/acs.organomet.5b00135
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6
Dual Gold Catalysis: Stepwise Catalyst Transfer via Dinuclear Clusters
Autor: K. N. Houk, A. Stephen K. Hashmi, Mie Højer Larsen
Publikováno v: Journal of the American Chemical Society. 137(33)
The interest in and use of dual gold catalysts is forever increasing, but little is known of the mechanism for the catalyst transfer and its effect on the continued high turnover frequency. Herein, we present a computational investigation of the mech
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88ee53f6b9f0f513466a65a4bbd6a813
https://pubmed.ncbi.nlm.nih.gov/26258807
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8
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