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- W1892316615 endingPage "2376" @default.
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- W1892316615 abstract "Alkylation reactions using alpha-halolactams or lactam enolates derived from bicyclic lactam templates can proceed with high endo- or exo- diastereoselectivity respectively. In the latter case, stereochemical correction by means of enolate generation and hindered phenol quench is possible with moderate efficiency. This protocol has been applied to the synthesis of protected penmacric acid and its analogues." @default.
- W1892316615 created "2016-06-24" @default.
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- W1892316615 date "2003-01-01" @default.
- W1892316615 modified "2023-10-03" @default.
- W1892316615 title "Pyrrolidinones derived from (S)-pyroglutamic acid: penmacric acid and analogues" @default.
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- W1892316615 doi "https://doi.org/10.1039/b303924b" @default.
- W1892316615 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/12945710" @default.
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