Synthesis of 2H-benzimidazole 1,3-dioxides, separase inhibitors, by reaction of o-benzoquinone dioximes with ketones

Synthesis of 2H-benzimidazole 1,3-dioxides, separase inhibitors, by reaction of o-benzoquinone dioximes with ketones Научная публикация

Журнал

Tetrahedron
ISSN: 0040-4020

Вых. Данные

Год: 2017, Том: 73, Номер: 27-28, Страницы: 3986-3992 Страниц : 7 DOI: 10.1016/j.tet.2017.05.078

Ключевые слова

2H-benzimidazole 1,3-dioxide; o-Benzoquinone dioxime; Ketone; Nitration; Separase inhibitor

Авторы

Chugunova Elena ^1,2 , Samsonov Vladimir ³ , Akylbekov Nurgali ⁴ , Mazhukin Dmitrii ^3,5

Организации

1	(Данные Web of science) Russian Acad Sci, AE Arbuzov Inst Organ & Phys Chem, Kazan Sci Ctr, 8 Arbuzov St, Kazan 420088, Russia
2	(Данные Web of science) Kazan Fed Univ, 18 Kremlyovskaya St, Kazan 420008, Russia
3	(Данные Web of science) Russian Acad Sci, Siberian Branch, NN Vorozhtsov Novosibirsk Inst Organ Chem, 9 Prosp Akad Lavrentreva, Novosibirsk 630090, Russia
4	(Данные Web of science) Kazan Natl Res Technol Univ, 68 Karl Marx St, Kazan 420015, Russia
5	(Данные Web of science) Novosibirsk State Univ, 2 Pirogova St, Novosibirsk 630090, Russia

The synthesis of novel 2H-benzimidazole 1,3-dioxides on the basis of o-benzoquinone dioximes interaction with ketones in the presence of acids is described. Nitration of these compounds by nitric acid in acetic acid yields the 5-nitro derivatives of 2H-benzimidazole 1,3-dioxide. (C) 2017 Elsevier Ltd. All rights reserved.

Chugunova E. , Samsonov V. , Akylbekov N. , Mazhukin D.
Synthesis of 2H-benzimidazole 1,3-dioxides, separase inhibitors, by reaction of o-benzoquinone dioximes with ketones
Tetrahedron. 2017. V.73. N27-28. P.3986-3992. DOI: 10.1016/j.tet.2017.05.078 WOS Scopus РИНЦ OpenAlex

Опубликована в печати:

1 июл. 2017 г.

Web of science:	WOS:000403998200024
Scopus:	2-s2.0-85019708401
РИНЦ:	31037667
OpenAlex:	W2620078510

БД	Цитирований
Web of science	4
Scopus	5
РИНЦ	4
OpenAlex	6