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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