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Cite the Following Article
A sustainable strategy for the straightforward preparation of 2H-azirines and highly functionalized NH-aziridines from vinyl azides using a single solvent flow-batch approach
Michael Andresini, Leonardo Degannaro and Renzo Luisi
Beilstein J. Org. Chem. 2021, 17, 203–209.
https://doi.org/10.3762/bjoc.17.20
How to Cite
Andresini, M.; Degannaro, L.; Luisi, R. Beilstein J. Org. Chem. 2021, 17, 203–209. doi:10.3762/bjoc.17.20
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- Dank, C.; Ielo, L. Recent advances in the accessibility, synthetic utility, and biological applications of aziridines. Organic & biomolecular chemistry 2023, 21, 4553–4573. doi:10.1039/d3ob00424d
- Vil', V. A.; Grishin, S. S.; Terent'ev, A. O. Electrochemically Induced Synthesis of Imidazoles from Vinyl Azides and Benzyl Amines. Molecules (Basel, Switzerland) 2022, 27, 7721. doi:10.3390/molecules27227721
- Sarkar, S.; De, A.; Santra, S.; Khalymbadzha, I. A.; Zyryanov, G. V.; Majee, A. Visible‐Light‐Mediated Synthesis of 1‐Oxa‐4‐aza‐spiro Oxazolines by Spiroannulation of Quinones with Vinyl Azides. European Journal of Organic Chemistry 2022, 2022. doi:10.1002/ejoc.202200503
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- Agafonova, A. V.; Smetanin, I. A.; Rostovskii, N. V.; Khlebnikov, A. F.; Novikov, M. S. Synthesis of 2-(2-Pyridyl)-2 H -azirines via Metal-Free C-C Cross-Coupling of Bromoazirines with 2-Stannylpyridines. Organic letters 2021, 23, 8045–8049. doi:10.1021/acs.orglett.1c03060