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Issue 10, 1985
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Stereospecific conversion of N,N-dimethylamphetamine into N-methylpseudoephedrine

Abstract

The pro-R hydrogen of (+)-N,N-dimethylamphetamine chromium tricarbonyl can be stereospecifically substituted via sequential treatment with BunLi and an electrophile, with rotation of configuration to give for example N-methylpseudoephedrine after decomplexation.

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Article type: Paper
DOI: 10.1039/C39850000653
Citation: J. Chem. Soc., Chem. Commun., 1985,0, 653-654
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    Stereospecific conversion of N,N-dimethylamphetamine into N-methylpseudoephedrine

    J. Blagg and S. G. Davies, J. Chem. Soc., Chem. Commun., 1985, 0, 653
    DOI: 10.1039/C39850000653

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