Efficient, Solvent-Free and Rapid Oxidation of Alcohols to Carbonyl Compounds with N,N'-Dibromo-N,N'-1,2-ethanediylbis(benzene sulfonamide)
Corresponding Author(s) : M. Mahboubifar
mahboubifar@yahoo.com
Asian Journal of Chemistry,
Vol. 23 No. 2 (2011): Vol 23 Issue 2
Abstract
N,N'-Dibromo-N,N'-1,2-ethanediylbis(benzene sulfonamide) (BNBBS): a safe, neutral and efficient reagent was utilized for the rapid and selective oxidation of alcohols to carbonyl compounds with no side reactions such as oxidations of carbon-hydrogen bonds, over oxidation of aldehydes and bromination of aromatic rings; under solvent-free condition, at room temperature with excellent yield.
Keywords
Solvent-free
Oxidation
Alcohols
Carbonyl compounds
N,N'-Dibromo-N,N'-1,2- ethanediylbis(benzene sulfonamide)
Mahboubifar, M., Khazaei, A., & Rostami, A. (2010). Efficient, Solvent-Free and Rapid Oxidation of Alcohols to Carbonyl Compounds with N,N’-Dibromo-N,N’-1,2-ethanediylbis(benzene sulfonamide). Asian Journal of Chemistry, 23(2), 829–831. Retrieved from https://asianpubs.org/index.php/ajchem/article/view/15872
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