Design of hetarylthiofuroxans by nucleophilic substitution of NO2 group in nitrofuroxans

Design of hetarylthiofuroxans by nucleophilic substitution of NO2 group in nitrofuroxans Научная публикация

Журнал

Mendeleev Communications
ISSN: 1364-551X , E-ISSN: 0959-9436

Вых. Данные

Год: 2015, Том: 25, Номер: 1, Страницы: 36-38 Страниц : 3 DOI: 10.1016/j.mencom.2015.01.013

Авторы

Fershtat Leonid L. ¹ , Epishina Margarita A. ¹ , Kulikov Alexander S. ¹ , Makhova Nina N. ¹

Организации

1	N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 119991 Moscow, Russian Federation

Hetarylthiofuroxans were synthesized by nucleophilic substitution of the nitro group in 4-nitrofuroxans under the action of hetarylthiols in the DBU–MeCN system at room temperature, reactivity of 4-nitrofuroxans being dependent on the C(3)-substituent.

Fershtat L.L. , Epishina M.A. , Kulikov A.S. , Makhova N.N.
Design of hetarylthiofuroxans by nucleophilic substitution of NO2 group in nitrofuroxans
Mendeleev Communications. 2015. V.25. N1. P.36-38. DOI: 10.1016/j.mencom.2015.01.013 WOS Scopus OpenAlex

≡ Web of science:	WOS:000349879400013
≡ Scopus:	2-s2.0-84921860316
≡ OpenAlex:	W2037092166