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- W2142565148 abstract "An atom-economic route to versatile building blocks: Vanadium enolates, which were generated in situ by the [3,3] sigmatropic rearrangement of vanadyl esters of allenic alcohols, undergo facile addition to imines derived from aromatic aldehydes to yield bifunctional β′-amino-α,β-unsaturated enones [Eq. (1)]. With 1,3-disubstituted allenes, good anti selectivity is observed in most cases." @default.
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- W2142565148 date "2003-05-08" @default.
- W2142565148 modified "2023-10-16" @default.
- W2142565148 title "Vanadium-Catalyzed anti-Selective Additions of Allenols to Imines" @default.
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- W2142565148 doi "https://doi.org/10.1002/anie.200350890" @default.
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