SCHEDULED MAINTENANCE
The 1,3-dipolar cycloaddition of the azomethine ylide (2) with homochiral cyclic dipolarophiles proceeds with high facial selectivity, whereas for homochiral acyclic dipolarophiles, the π-facial selectivity and mode of cycloaddition is dependent on the structure of the dipolarophile.
A. G. H. Wee, J. Chem. Soc., Perkin Trans. 1, 1989, 1363 DOI: 10.1039/P19890001363
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