A Rapid and Convenient Synthesis of a-Diketones
Corresponding Author(s) : Dong-Zhi Liu
sjz_wgq@126.com
Asian Journal of Chemistry,
Vol. 23 No. 1 (2011): Vol 23 Issue 1
Abstract
A novel and simple synthetic method for the preparation of series of a-diketones is reported. a-Ditrimethylsiloxyenes were obtained from the readily available materials diacids or diesters through acyloin condensation, which was oxidized to a-diketones using bromine as the oxidation reagent in presence of water. The structures of a-diketones were confirmed by IR, MS, 1H NMR.
Keywords
Acyloin condensation
Oxidation
Synthesis
α-Diketones
Chen, S.-R., Ma, J.-H., Zhou, X.-Q., & Liu, D.-Z. (2010). A Rapid and Convenient Synthesis of a-Diketones. Asian Journal of Chemistry, 23(1), 467–468. Retrieved from https://asianpubs.org/index.php/ajchem/article/view/10074
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