Enviar artigo por via de e-mail N-Sulfinyltrifluoromethanesulfonamide in [4+2]-Cycloaddition Reactions
- Autores: Tolstikova L.L1, Astakhova V.V1, Moskalik M.Y.1
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Afiliações:
- Federal Research Center "Irkutsk Institute of Chemistry named after A.E. Favorsky", Siberian Branch of the Russian Academy of Sciences
- Edição: Volume 95, Nº 11-12 (2025)
- Páginas: 554-561
- Seção: Articles
- URL: https://bakhtiniada.ru/0044-460X/article/view/362181
- DOI: https://doi.org/10.7868/S3034559625110108
- ID: 362181
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Resumo
The reaction of N-sulfinyltrifluoromethanesulfonamide with acyclic conjugated dienes in methylene chloride was shown to afford the corresponding cycloadducts in high yields. Methyl vinyl ketone reacted with N-sulfinyltrifluoromethanesulfonamide in the presence of thionyl chloride, also affording the cycloaddition product, while terminal alkenes in this reaction give the corresponding sulfinamides.
Sobre autores
L. Tolstikova
Federal Research Center "Irkutsk Institute of Chemistry named after A.E. Favorsky", Siberian Branch of the Russian Academy of Sciences
ORCID ID: 0000-0002-0530-7429
V. Astakhova
Federal Research Center "Irkutsk Institute of Chemistry named after A.E. Favorsky", Siberian Branch of the Russian Academy of Sciences
Email: astakhova_vera@irioch.irk.ru
ORCID ID: 0000-0001-9716-6004
M. Moskalik
Federal Research Center "Irkutsk Institute of Chemistry named after A.E. Favorsky", Siberian Branch of the Russian Academy of Sciences
ORCID ID: 0000-0002-9460-3413
Bibliografia
- Веремейчик Ю.В., Шуринк Д.Н., Лодочникова О.А., Племенков В.В. // ЖОХ. 2016. T. 86. № 2. C. 268. @@ Verenreichik Y.V., Shurpik D.N., Lodochnikova O.A., Plemenkov V.V. // Russ. J. Gen. Chem. 2016. Vol. 86. P. 296. doi: 10.1134/S1070363216020158
- Шаинян Б.А., Толстикова Л.Л. // ЖОРХ. 2016. T. 52. № 4. C. 511 @@ Shainyan B.A., Tolstikova L.L. // Russ. J. Org. Chem. 2016. Vol. 52. N 4. P. 499. doi: 10.1134/S1070428016040035
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