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

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

Fingerprint Подробные сведения о темах исследования «Synthesis of 1,2,4-thiadiazoles by oxidative dimerization of carbothioamides by using oxone». Вместе они формируют уникальный семантический отпечаток (fingerprint).

Цитировать

Yoshimura, A., Todora, A. D., Kastern, B. J., Koski, S. R., & Zhdankin, V. V. (2014). Synthesis of 1,2,4-thiadiazoles by oxidative dimerization of carbothioamides by using oxone. European Journal of Organic Chemistry, 2014(24), 5149-5152. https://doi.org/10.1002/ejoc.201402756

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

@article{861a2f6c6814463b9bc933d7c720ceb1,

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

abstract = "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.",

keywords = "Heterocycles, Oxidation, Oxone, Selenium, Sulfur",

author = "Akira Yoshimura and Todora, {Anthony D.} and Kastern, {Brent J.} and Koski, {Steven R.} and Zhdankin, {Viktor V.}",

year = "2014",

month = jan,

day = "1",

doi = "10.1002/ejoc.201402756",

language = "English",

volume = "2014",

pages = "5149--5152",

journal = "Annalen der Pharmacie",

issn = "0075-4617",

publisher = "Wiley-VCH Verlag",

number = "24",

}

TY - JOUR

T1 - Synthesis of 1,2,4-thiadiazoles by oxidative dimerization of carbothioamides by using oxone

AU - Yoshimura, Akira

AU - Todora, Anthony D.

AU - Kastern, Brent J.

AU - Koski, Steven R.

AU - Zhdankin, Viktor V.

PY - 2014/1/1

Y1 - 2014/1/1

N2 - 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.

AB - 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.

KW - Heterocycles

KW - Oxidation

KW - Oxone

KW - Selenium

KW - Sulfur

UR - http://www.scopus.com/inward/record.url?scp=84906057516&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84906057516&partnerID=8YFLogxK

U2 - 10.1002/ejoc.201402756

DO - 10.1002/ejoc.201402756

M3 - Article

AN - SCOPUS:84906057516

VL - 2014

SP - 5149

EP - 5152

JO - Annalen der Pharmacie

JF - Annalen der Pharmacie

SN - 0075-4617

IS - 24

ER -