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

Standard

Synthesis of 2H-benzimidazole 1,3-dioxides, separase inhibitors, by reaction of o-benzoquinone dioximes with ketones. / Chugunova, Elena; Samsonov, Vladimir; Akylbekov, Nurgali и др.

в: Tetrahedron, Том 73, № 27-28, 06.07.2017, стр. 3986-3992.

Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование

Harvard

Chugunova, E, Samsonov, V, Akylbekov, N & Mazhukin, D 2017, 'Synthesis of 2H-benzimidazole 1,3-dioxides, separase inhibitors, by reaction of o-benzoquinone dioximes with ketones', Tetrahedron, Том. 73, № 27-28, стр. 3986-3992. https://doi.org/10.1016/j.tet.2017.05.078

APA

Chugunova, E., Samsonov, V., Akylbekov, N., & Mazhukin, D. (2017). Synthesis of 2H-benzimidazole 1,3-dioxides, separase inhibitors, by reaction of o-benzoquinone dioximes with ketones. Tetrahedron, 73(27-28), 3986-3992. https://doi.org/10.1016/j.tet.2017.05.078

Vancouver

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 июль 6;73(27-28):3986-3992. doi: 10.1016/j.tet.2017.05.078

Author

Chugunova, Elena ; Samsonov, Vladimir ; Akylbekov, Nurgali и др. / Synthesis of 2H-benzimidazole 1,3-dioxides, separase inhibitors, by reaction of o-benzoquinone dioximes with ketones. в: Tetrahedron. 2017 ; Том 73, № 27-28. стр. 3986-3992.

BibTeX

@article{44b11ead35414fc884c9a450c597bbe8,

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

abstract = "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.",

keywords = "2H-benzimidazole 1,3-dioxide, Ketone, Nitration, o-Benzoquinone dioxime, Separase inhibitor, DERIVATIVES",

author = "Elena Chugunova and Vladimir Samsonov and Nurgali Akylbekov and Dmitrii Mazhukin",

note = "Publisher Copyright: {\textcopyright} 2017 Elsevier Ltd",

year = "2017",

month = jul,

day = "6",

doi = "10.1016/j.tet.2017.05.078",

language = "English",

volume = "73",

pages = "3986--3992",

journal = "Tetrahedron",

issn = "0040-4020",

publisher = "Elsevier",

number = "27-28",

}

RIS

TY - JOUR

T1 - Synthesis of 2H-benzimidazole 1,3-dioxides, separase inhibitors, by reaction of o-benzoquinone dioximes with ketones

AU - Chugunova, Elena

AU - Samsonov, Vladimir

AU - Akylbekov, Nurgali

AU - Mazhukin, Dmitrii

PY - 2017/7/6

Y1 - 2017/7/6

N2 - 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.

AB - 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.

KW - 2H-benzimidazole 1,3-dioxide

KW - Ketone

KW - Nitration

KW - o-Benzoquinone dioxime

KW - Separase inhibitor

KW - DERIVATIVES

UR - http://www.scopus.com/inward/record.url?scp=85019708401&partnerID=8YFLogxK

U2 - 10.1016/j.tet.2017.05.078

DO - 10.1016/j.tet.2017.05.078

M3 - Article

AN - SCOPUS:85019708401

VL - 73

SP - 3986

EP - 3992

JO - Tetrahedron

JF - Tetrahedron

SN - 0040-4020

IS - 27-28

ER -

ID: 10191441