Aerobic oxidation at benzylic positions catalyzed by a simple Pd(OAc) 2 /bis-triazole system

An efficient catalyst system for the Pd-catalyzed aerobic oxidation of benzylic positions has been developed. The combination of palladium( ii ) acetate and 3,5-bis((1 H -1,2,4-triazol-1-yl)methyl)benzoate ligand allows the selective oxidation at carbon adjacent to arene rings (primary and secondary...

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Published inRSC advances Vol. 5; no. 125; pp. 103210 - 103217
Main Authors Urgoitia, Garazi, Maiztegi, Ainhoa, SanMartin, Raul, Herrero, María Teresa, Domínguez, Esther
Format Journal Article
LanguageEnglish
Published 01.01.2015
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Summary:An efficient catalyst system for the Pd-catalyzed aerobic oxidation of benzylic positions has been developed. The combination of palladium( ii ) acetate and 3,5-bis((1 H -1,2,4-triazol-1-yl)methyl)benzoate ligand allows the selective oxidation at carbon adjacent to arene rings (primary and secondary benzylic alcohols, and other benzyl compounds) to provide the corresponding carbonyl and carboxy derivatives, employing molecular oxygen as oxidizing agent and a very low metal loading (10 −5 mol%).
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ISSN:2046-2069
2046-2069
DOI:10.1039/C5RA22251F