Research output: Contribution to journal › Article › peer-review
The oxidative phthalimidoaziridination of conjugated unsaturated N-sulfonylimines leads, in most cases, to di-substituted, tri-substituted and spiro-fused imidoylaziridines in synthetically useful yields typically above 70 %. The latter are thermally transformed into di-substituted, tri-substituted, and condensed N-sulfonylimidazoles. Interestingly, this ring expansion is accompanied by an intramolecular 1,3-sulfonyl shift from one nitrogen atom to another.
Translated title of the contribution | Термическое расширение цикла 2-сульфонилимидоил-1-фталимидоазиридинов в N-сульфонилимидазолы |
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Original language | English |
Pages (from-to) | 1634-1645 |
Number of pages | 12 |
Journal | European Journal of Organic Chemistry |
Volume | 2018 |
Issue number | 14 |
DOIs | |
State | Published - 17 Apr 2018 |
ID: 35787330