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- W2085080302 endingPage "2017" @default.
- W2085080302 startingPage "2010" @default.
- W2085080302 abstract "The Staudinger ketene-imine reaction between ketenes generated from natural O,N-protected trans-4-hydroxy-l-prolines and the N-benzyl-N-benzylideneamine led to mixtures of diastereoisomeric, enantiomerically pure pyrrolidine-derived spiro-beta-lactams with a relative cis configuration. These were transformed into the corresponding pyrroline-spiro-beta-lactams by means of treatment with a base and the new C=C double bond was submitted to a number of different reactions in order to evaluate its reactivity and obtain new polyheterocyclic enantiomerically pure spiro-beta-lactams." @default.
- W2085080302 created "2016-06-24" @default.
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- W2085080302 creator A5034428791 @default.
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- W2085080302 date "2010-02-26" @default.
- W2085080302 modified "2023-10-06" @default.
- W2085080302 title "Enantiomerically Pure Polyheterocyclic Spiro-β-lactams from <i>trans</i>-4-Hydroxy-<scp>l</scp>-proline" @default.
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- W2085080302 doi "https://doi.org/10.1021/jo100061s" @default.
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