Мақаланы E-mail арқылы жіберу N-Sulfinyltrifluoromethanesulfonamide in [4+2]-Cycloaddition Reactions
- Авторлар: Tolstikova L.L1, Astakhova V.V1, Moskalik M.Y.1
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Мекемелер:
- Federal Research Center "Irkutsk Institute of Chemistry named after A.E. Favorsky", Siberian Branch of the Russian Academy of Sciences
- Шығарылым: Том 95, № 11-12 (2025)
- Беттер: 554-561
- Бөлім: Articles
- URL: https://bakhtiniada.ru/0044-460X/article/view/362181
- DOI: https://doi.org/10.7868/S3034559625110108
- ID: 362181
Дәйексөз келтіру
Ашық рұқсат
Рұқсат берілді
Тек жазылушылар үшін
Аннотация
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.
Авторлар туралы
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
Әдебиет тізімі
- 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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