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Issue 9, 2010
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Synthesis of oxazolidinones initiated by regio- and diastereo-controlled crotylation of α-dicarbonyl compounds

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Abstract

A one-pot synthesis of oxazolidinones was initiated via the allylation of α-dicarbonyl compounds, accompanying regio- and diastereo-controlled carboncarbon bond formation on the side chains of the oxazolidinones.

Graphical abstract: Synthesis of oxazolidinones initiated by regio- and diastereo-controlled crotylation of α-dicarbonyl compounds

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Publication details

The article was received on 14 Jan 2010, accepted on 09 Mar 2010 and first published on 16 Mar 2010


Article type: Communication
DOI: 10.1039/C000197J
Org. Biomol. Chem., 2010,8, 2009-2011

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    Synthesis of oxazolidinones initiated by regio- and diastereo-controlled crotylation of α-dicarbonyl compounds

    I. Shibata, R. Kojima, S. Tsunoi, T. Nozaki, T. Watanabe, A. Ninomiya, M. Yasuda and A. Baba, Org. Biomol. Chem., 2010, 8, 2009
    DOI: 10.1039/C000197J

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