Synthesis of 1,2,4-thiadiazoles by oxidative dimerization of carbothioamides by using oxone

Akira Yoshimura, Anthony D. Todora, Brent J. Kastern, Steven R. Koski, Viktor V. Zhdankin

Результат исследований: Материалы для журнала › Статья

18 Цитирования (Scopus)

Выдержка

1,2,4-Thiadiazoles were efficiently synthesized in good yields through the oxidative dimerization of carbothioamides by using Oxone as a readily available, inexpensive, and environmentally safe oxidant. A similar reaction of phenylselenoamide led to the corresponding 1,2,4-phenylselenadiazole in high yield.

Язык оригиналаАнглийский
Страницы (с-по)5149-5152
Число страниц4
ЖурналEuropean Journal of Organic Chemistry
Том2014
Номер выпуска24
DOI
СостояниеОпубликовано - 1 янв 2014
Опубликовано для внешнего пользованияДа

Отпечаток

Thiadiazoles
Dimerization
dimerization
Oxidants
synthesis
potassium peroxymonosulfuric acid

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry
  • Organic Chemistry

Цитировать

Synthesis of 1,2,4-thiadiazoles by oxidative dimerization of carbothioamides by using oxone. / Yoshimura, Akira; Todora, Anthony D.; Kastern, Brent J.; Koski, Steven R.; Zhdankin, Viktor V.

В: European Journal of Organic Chemistry, Том 2014, № 24, 01.01.2014, стр. 5149-5152.

Результат исследований: Материалы для журнала › Статья

Yoshimura, A, Todora, AD, Kastern, BJ, Koski, SR & Zhdankin, VV 2014, 'Synthesis of 1,2,4-thiadiazoles by oxidative dimerization of carbothioamides by using oxone', European Journal of Organic Chemistry, том. 2014, № 24, стр. 5149-5152. https://doi.org/10.1002/ejoc.201402756
Yoshimura A, Todora AD, Kastern BJ, Koski SR, Zhdankin VV. Synthesis of 1,2,4-thiadiazoles by oxidative dimerization of carbothioamides by using oxone. European Journal of Organic Chemistry. 2014 Янв. 1;2014(24):5149-5152. https://doi.org/10.1002/ejoc.201402756
Yoshimura, Akira ; Todora, Anthony D. ; Kastern, Brent J. ; Koski, Steven R. ; Zhdankin, Viktor V. / Synthesis of 1,2,4-thiadiazoles by oxidative dimerization of carbothioamides by using oxone. В: European Journal of Organic Chemistry. 2014 ; Том 2014, № 24. стр. 5149-5152.
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