Abstract
Cycloaddition reactions of aziridines with dipolarophiles under traditional thermal or photochemical conditions entail destructive routes to form reactive intermediates such as an azomethine ylide. This article highlights a recent study that demonstrates a cycloaddition reaction of aziridine induced by mechanical force. Experimental results suggest that the force-induced cycloaddition of aziridine with dimethyl acetylenedicarboxylate as a dipolarophile does not seem to involve an ylide, with implications for a possible new reaction route.1 Rivalry between Aziridine and Epoxide2 Mechanochemically Responsive Polymers3 Aziridine Mechanophore4 Concluding Remarks and Outlook
Funder
National Research Foundation of Korea
Cited by
6 articles.
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