Publikace: Recent advances in palladium-catalysed asymmetric 1,4-additions of arylboronic acids to conjugated enones and chromones
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Bartáček, Jan
Svoboda, Jan
Kocúrik, Martin
Pochobradský, Jaroslav
Čegan, Alexander
Sedlák, Miloš
Váňa, Jiří
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Beilstein-Institut
Abstrakt
The transition metal (palladium)-catalysed asymmetric 1,4-addition of arylboronic acids to conjugated enones belong to the most important and emerging strategies for the construction of C-C bonds in an asymmetric fashion. This review covers known catalytic systems used for this transformation. For clarity, we are using the type of ligand as a sorting criterion. Finally, we attempted to create a flowchart facilitating the selection of a suitable ligand for a given combination of enone and arylboronic acid.
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Klíčová slova
asymmetric reaction, arylboronic acids, conjugated enones, chromones, enantioselective catalysis, Michael addition, Pd complexes, asymetrická reakce, arylboronové kyseliny, konjugované enony, chromony, enantioselektivní katalýza, Michaelova adice, Pd komplexy