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pro vyhledávání: '"Ingolf Harden"'
Publikováno v:
Chemical science. 13(30)
We elucidate the stereo-controlling factors of the asymmetric intramolecular hydroalkoxylation of terminal olefins catalyzed by bulky Brønsted acids [
Autor:
Sayanti Chatterjee, Ingolf Harden, Giovanni Bistoni, Rebeca G. Castillo, Sonia Chabbra, Maurice van Gastel, Alexander Schnegg, Eckhard Bill, James A. Birrell, Bill Morandi, Frank Neese, Serena DeBeer
Publikováno v:
Journal of the American Chemical Society, 144 (6)
Journal of the American Chemical Society 144(6), 2637-2656 (2022). doi:10.1021/jacs.1c11083
Journal of the American Chemical Society 144(6), 2637-2656 (2022). doi:10.1021/jacs.1c11083
Herein, we study the mechanism of iron-catalyzed direct synthesis of unprotected aminoethers from olefins by a hydroxyl amine derived reagent using a wide range of analytical and spectroscopic techniques (Mössbauer, Electron Paramagnetic Resonance,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b678ba94c3df1c7b0ed69dd9a53a6f91
https://hdl.handle.net/20.500.11850/535507
https://hdl.handle.net/20.500.11850/535507
We elucidate the stereo-controlling factors of the asymmetric intramolecular hydroalkoxylation of terminal olefins catalyzed by bulky Brønsted acids [Science2018, 359 (6383), 1501–1505] using high-level electronic structure methods.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7530e0ecf84a6f3864bd9e755679552e
https://hdl.handle.net/11391/1544833
https://hdl.handle.net/11391/1544833
Autor:
Benjamin Mitschke, Chandra Kanta De, Giovanni Bistoni, Sayantani Das, Ingolf Harden, Benjamin List
Publikováno v:
Nature Catalysis
Nitronate anions, formally generated by α-deprotonating the corresponding nitroalkanes, are highly nucleophilic and versatile intermediates in many carbon–carbon bond-forming reactions. In contrast, the corresponding silyl nitronates are ambiphili
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc3d14a32dc361eea312313efba48d85
https://hdl.handle.net/21.11116/0000-0009-A608-321.11116/0000-000A-6C32-5
https://hdl.handle.net/21.11116/0000-0009-A608-321.11116/0000-000A-6C32-5