
TY  - JOUR
A1  - Duewell, H 
T1  - 1,3-Dipolar cycloaddition of <I>cis</I>-2,3-Dibenzoyl-1-phenylaziridine
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1977
VL  - 30
IS  - 6
SP  - 1367
EP  - 1374
KW  - 
UR  - https://doi.org/10.1071/CH9771367 
N2  - 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. 
ER  -

