Abstract
The 1,3-dipolar cycloaddition reaction can generate four stereocenters with defined stereochemistry in a single step. The authors report on the reaction of azomethine ylides with N-methylmaleimide as dipolarophile in the presence of a chiral silver catalyst. The catalyst itself is insoluble in the reaction solvent and can be recovered and used consecutively up to four times with minimal loss in activity and selectivity.
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