Palladium-catalyzed anti-Markovnikov oxidative acetalization of activated olefins with iron(iii ) sulphate as the reoxidant
Autor: | Rodney A. Fernandes, Sandhya S. Yadav, Praveen Kumar |
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Rok vydání: | 2022 |
Předmět: | |
Zdroj: | Organic & Biomolecular Chemistry. 20:427-443 |
ISSN: | 1477-0539 1477-0520 |
DOI: | 10.1039/d1ob02227j |
Popis: | This paper discloses the efficient palladium-catalyzed anti-Markovnikov oxidative acetalization of activated terminal olefins with iron(III) sulfate as the reoxidant. This methodology requires mild reaction conditions and shows high regioselectivity toward anti-Markovnikov products and compatibility with a wide range of functional groups. Iron(III) sulphate was the sole reoxidant used in this method. Various olefins like vinylarenes, aryl-allylethers, aryl or benzyl acrylates and homoallylic alcohols all reacted well providing anti-Markovnikov acetals, some of which represent orthogonally functionalized 1,3- and 1,4-dioxygenated compounds. |
Databáze: | OpenAIRE |
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