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Force-Induced Cycloaddition of Aziridine: Can We Force a New Route?

Authors
Jung, SangminKim, Seo YeonYoon, Hyo Jae
Issue Date
1-9월-2020
Publisher
GEORG THIEME VERLAG KG
Keywords
aziridines; cycloaddition; mechanochemistry; mechanophores; stereoselectivity
Citation
SYNLETT, v.31, no.14, pp.1343 - 1348
Indexed
SCIE
SCOPUS
Journal Title
SYNLETT
Volume
31
Number
14
Start Page
1343
End Page
1348
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/53213
DOI
10.1055/s-0040-1707145
ISSN
0936-5214
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
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