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- W2951566119 abstract "Abstract The aza-annulation of an acyclic β-enaminoester with acryloyl chloride was found to be a very efficient method for nitrogen heterocycle formation. Stereospecific hydrogenation of the unsaturated dihydropyridone generated from aza-annulation gave a single disubstituted lactam product. The cis stereochemical relationship of the substituents was confirmed by transformation of the lactam to (±)-lupinine." @default.
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- W2951566119 date "2010-08-20" @default.
- W2951566119 modified "2023-09-26" @default.
- W2951566119 title "ChemInform Abstract: Heterocycle Formation Through Aza-Annulation: A Stereochemically Controlled Route to (.+-.)-Lupinine." @default.
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- W2951566119 doi "https://doi.org/10.1002/chin.199323278" @default.
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