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- W2076571494 abstract "Stable configuration of ester-stabilized azomethine ylides is found to depend upon the substituent on the ylide nitrogen. Thus, N-substituted azomethine ylides derived from N-substituted 2-aminoacetates and carbonyl compounds undergo cycloaddition with olefinic dipolarophiles predominantly in anti forms, while N-protonated (or N-unsubstituted) azomethine ylides generated from 2-iminoacetates exclusively in syn forms." @default.
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- W2076571494 date "1986-08-05" @default.
- W2076571494 modified "2023-09-27" @default.
- W2076571494 title "Stable Configuration of Ester-Stabilized Azomethine Ylides. Stabilization ofanti-Form by 1,5-Dipolar Interaction and ofsyn-Form by Hydrogen Bonding" @default.
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- W2076571494 doi "https://doi.org/10.1246/cl.1986.1271" @default.
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