Abstract
Various chiral α,β-unsaturated γ-lactams 1 were prepared in high yield and in a single step from corresponding primary amines. The different reactivities of lactams 1 could be exploited to prepare diversely substituted pyrrolidones, pyrrolidines, γ-aminoacids and alkaloids. Their application to the synthesis of enantiomerically pure (-)-cephalotaxine are described. ©ARKAT.
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APA
Baussanne, I., Dudot, B., Pérard-Viret, J., Planas, L., & Royer, J. (2005, December 30). New developments in the asymmetric synthesis of heterocyclic natural products. Arkivoc. https://doi.org/10.3998/ark.5550190.0007.706
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