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 Epoxide 2 Mechanochemically Responsive Polymers 3 Aziridine Mechanophore 4 Concluding Remarks and Outlook.
Original language | English |
---|---|
Article number | st-2020-p0283-sp |
Pages (from-to) | 1343-1348 |
Number of pages | 6 |
Journal | Synlett |
Volume | 31 |
Issue number | 14 |
DOIs | |
Publication status | Published - 2020 Sept 1 |
Keywords
- Aziridines
- cycloaddition
- mechanochemistry
- mechanophores
- stereoselectivity
ASJC Scopus subject areas
- Organic Chemistry