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A new and versatile one-pot strategy to synthesize alpha-bromoketones from secondary alcohols using ammonium bromide and oxone

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Abstract

A new, efficient and green protocol for the one-pot synthesis of α-bromoketones from secondary alcohols using cheap, air stable and non-toxic reagents such as NH4Br and oxone has been developed. This reaction proceeds via two consecutive steps such as oxidation of secondary alcohols and oxidative bromination of in situ generated ketones.

Graphical abstract: A new and versatile one-pot strategy to synthesize alpha-bromoketones from secondary alcohols using ammonium bromide and oxone

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Publication details

The article was received on 05 Jan 2017, accepted on 05 Apr 2017 and first published on 06 Apr 2017


Article type: Letter
DOI: 10.1039/C7NJ00052A
Citation: New J. Chem., 2017, Advance Article
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    A new and versatile one-pot strategy to synthesize alpha-bromoketones from secondary alcohols using ammonium bromide and oxone

    B. Rammurthy, P. Swamy, M. Naresh, K. Srujana, C. Durgaiah, G. Krishna Sai and N. Narender, New J. Chem., 2017, Advance Article , DOI: 10.1039/C7NJ00052A

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