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À propos de : Asymmetric Amine-Intercepted Nazarov Cyclization        

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  • Asymmetric Amine-Intercepted Nazarov Cyclization
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  • The chiral auxiliary directed addition of a propargyllithium reagent to a morpholino enamide, followed by exposure of the adduct to activated dry Florisil in the absence of solvent and in the presence of a primary or secondary amine, leads to a cascade of reactions that results in the formation of an aminocyclopentenone as a single diastereoisomer. The reaction can also be conducted intramolecularly.
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