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Abstract
The conjugate addition of a homochiral lithium amide to a ξ-hydroxy-α,β-unsaturated ester, tollowed by a one-pot, ring-closure-N-debenzylation protocol has been used in the asymmetric syntheses of (S)-coniine and (R)-δ-coniceine (isolated as the corresponding hydrochloride salts) and the bicyclic core of stellettamide A.
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