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- W2950784647 abstract "The azomethine ylides, formed by treatment of the N-oxides (II), (VI), or (XIV) with LDA, are subjected in situ to cycloaddition reaction with various dipolarophiles, e.g. (I), (IX), (XI), or (XV), producing pyrrole derivatives such as (III) - (V), (VII), (VIII), and (X), the tetrahydrothiazoles (XII) and (XIII), or the fused piperidines (XVI) and (XVII)." @default.
- W2950784647 created "2019-06-27" @default.
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- W2950784647 date "1989-02-07" @default.
- W2950784647 modified "2023-09-25" @default.
- W2950784647 title "ChemInform Abstract: Study of the Regiochemistry and Stereochemistry of the (3 + 2)Cycloaddition Between Nonstabilized Azomethine Ylides Generated from Tertiary Amine N-Oxides and Various Dipolarophiles." @default.
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- W2950784647 doi "https://doi.org/10.1002/chin.198906089" @default.
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