Abstract
Abstract Palladium-catalyzed allylations of (S)-proline allyl ester amides are discussed, compared with the intermolecular reactions of (S)-proline methyl and ethyl ester amides with allyl acetate. (S)-Proline allyl ester amide undergoes an intramolecular allylation to demonstrate higher diastereoselectivity than the other systems, upon treatment with palladium catalysts.
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