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Five- and six-membered nitrogen and oxygen heterocycles are accessible from two acyclic precursors in a one-pot reaction that comprises a Ru-catalyzed ene–yne addition followed by a Pd-catalyzed asymmetric allylic alkylation (see scheme). The stereochemistry of the products derives from the catalyst rather than from substrate control using chiral substrates.
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Trost et al. (2002) studied this question.
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