Organic Letters
Letter
(5) Intramolecular aziridination was mostly limited to the synthesis
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of [3.1.0] and [4.1.0] bicyclic aziridines; see: (a) Muller, P.; Baud, C.;
ASSOCIATED CONTENT
* Supporting Information
The Supporting Information is available free of charge on the
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Experimental details and characterization data for all
AUTHOR INFORMATION
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Corresponding Author
ORCID
Notes
(6) In the synthesis of [4.1.0] bicyclic aziridines, a few [5.1.0]
sulfonated bicyclic aziridines were reported; see: (a) Duran, F.;
Leman, L.; Ghini, A.; Burton, G.; Dauban, P.; Dodd, R. H. Org. Lett.
The authors declare no competing financial interest.
2002, 4, 2481. (b) Fruit, C.; Muller, P. Tetrahedron: Asymmetry 2004,
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ACKNOWLEDGMENTS
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15, 1019. (c) Guthikonda, K.; Wehn, P. M.; Caliando, B. J.; Du Bois,
J. Tetrahedron 2006, 62, 11331. (d) Esteoule, A.; Duran, F.;
Retailleau, P.; Dodd, R. H.; Dauban, P. Synthesis 2007, 2007, 1251.
(e) Kurokawa, T.; Kim, M.; Du Bois, J. Angew. Chem., Int. Ed. 2009,
48, 2777. (f) Fiori, K. W.; Espino, C. G.; Brodsky, B. H.; Du Bois, J.
Tetrahedron 2009, 65, 3042. (g) Kornecki, K. P.; Berry, J. F.; Hoque,
M. M.; Miyamoto, K.; Tada, N.; Shiro, M.; Ochiai, M. Chem.
Commun. 2012, 48, 12097.
We acknowledge financial support from the National Natural
Science Foundation of China (21472085, 21332005,
21672100) and the Fundamental Research Funds for the
Central Universities (020514380131).
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