Abstract
trans-4-Hydroxy- l-proline is used for the first time as an effective nucleophilic coupling partner with aryl halides mediated by copper iodide with Cs 2CO 3 as the base and DMSO as the solvent. Utilizing this protocol cross-coupling of trans-4-hydroxy- l-proline with a wide variety of substituted aryl halides to produce N-aryl pyrroles in moderate to good yields.
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