Chiral amine-induced stereoselectivity in trans-β-lactam formation via Staudinger cycloaddition

A series of chiral trans-β-lactams was obtained via Staudinger cycloaddition with low to moderate diastereoselectivity (up to 54% de) induced by a chiral amine component of the imine. It was shown that the direct connection of nitrogen to a chiral centre is crucial to induce chirality; moderate asymmetric induction was achieved by using isomeric 1-phenylethylamines, which are among the cheapest chiral sources on the market, while low diastereoselectivity was obtained from 3-aminomethylpinane, where the chiral centres are distant from nitrogen by a methylene group. It was shown, that an increase of the reaction temperature from 110 °C to 140 °C led to commensurable results but speeded-up the transformation significantly. The absolute configurations of phenylethylamine derivatives were determined by X-ray analysis of selected samples.

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