The construction of a hybrid metal-organo-photoredox catalyst based on the conjugation of an imidazolidinone organocatalyst and Ir(ppy)2(bipy) (ppy = 2-phenylpyridine, bipy = bipyridine) is described. The introduction of the desired organocatalyst into the bipyridine moiety is quite modular, allowing the preparation of different hybrid photocatalysts, and is realized though a simple click reaction. The hybrid photocatalysts obtained were employed in the benchmark photoredox alkylation of aldehydes. Remarkably, the conjugation of a first-generation MacMillan catalyst produces an active and stereoselective hybrid photoredox catalyst.
Gualandi, A., Calogero, F., Martinelli, A., Quintavalla, A., Marchini, M., Ceroni, P., et al. (2020). A supramolecular bifunctional iridium photoaminocatalyst for the enantioselective alkylation of aldehydes. DALTON TRANSACTIONS, 49(41), 14497-14505-14505 [10.1039/d0dt02587a].
A supramolecular bifunctional iridium photoaminocatalyst for the enantioselective alkylation of aldehydes
Gualandi, Andrea
;Calogero, Francesco;Martinelli, Ada;Quintavalla, Arianna;Marchini, Marianna;Ceroni, Paola
;Lombardo, Marco
;Cozzi, Pier Giorgio
2020
Abstract
The construction of a hybrid metal-organo-photoredox catalyst based on the conjugation of an imidazolidinone organocatalyst and Ir(ppy)2(bipy) (ppy = 2-phenylpyridine, bipy = bipyridine) is described. The introduction of the desired organocatalyst into the bipyridine moiety is quite modular, allowing the preparation of different hybrid photocatalysts, and is realized though a simple click reaction. The hybrid photocatalysts obtained were employed in the benchmark photoredox alkylation of aldehydes. Remarkably, the conjugation of a first-generation MacMillan catalyst produces an active and stereoselective hybrid photoredox catalyst.File | Dimensione | Formato | |
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