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 › рецензирование

Аннотация

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 оригинала	Английский
Страницы (с-по)	5149-5152
Число страниц	4
Журнал	European Journal of Organic Chemistry
Том	2014
Номер выпуска	24
DOI	https://doi.org/10.1002/ejoc.201402756
Состояние	Опубликовано - 1 янв 2014
Опубликовано для внешнего пользования	Да

ASJC Scopus subject areas

Physical and Theoretical Chemistry
Organic Chemistry

Доступ к документу

10.1002/ejoc.201402756

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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 › рецензирование

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