Cycloaddition of an aziridine to ketens
- 1 January 1972
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 3,p. 199-200
- https://doi.org/10.1039/c39720000199
Abstract
The azomethine ylide arising from the cleavage of dimethyl 1,3-diphenylaziridine-2,2-dicarboxylate adds preferentially to the CO bond of ketens to give 5-methyleneoxazolidines with two ester groups on C(4).Keywords
This publication has 0 references indexed in Scilit: