Abstract
Cis-2,3-Dibenzoyl-1-phenylaziridine is highly reactive in 1,3-dipolar cycloadditions. Reactions with dimethyl fumarate and with dimethyl maleate at 125�C yield together all possible isomeric dimethyl 2,5- dibenzoyl-1-phenylpyrrolidine-3,4-dicarboxylates. Cycloadditions with reactive dipolarophiles at 85�C lead to adducts derived from the parent aziridine without isomerization of the intermediate ylid.

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