| Literature DB >> 24009102 |
Jia Jia Dong1, Duenpen Unjaroen, Francesco Mecozzi, Emma C Harvey, Pattama Saisaha, Dirk Pijper, Johannes W de Boer, Paul Alsters, Ben L Feringa, Wesley R Browne.
Abstract
An efficient and simple method for selective oxidation of secondary alcohols and oxidation of alkanes to ketones is reported. An in situ prepared catalyst is employed based on manganese(II) salts, pyridine-2-carboxylic acid, and butanedione, which provides good-to-excellent conversions and yields with high turnover numbers (up to 10 000) with H2 O2 as oxidant at ambient temperatures. In substrates bearing multiple alcohol groups, secondary alcohols are converted to ketones selectively and, in general, benzyl C-H oxidation proceeds in preference to aliphatic C-H oxidation.Entities:
Keywords: alcohol oxidation; alkane oxidation; catalysis; manganese
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Year: 2013 PMID: 24009102 DOI: 10.1002/cssc.201300378
Source DB: PubMed Journal: ChemSusChem ISSN: 1864-5631 Impact factor: 8.928