Research output: Contribution to journal › Article › peer-review
Synthesis of 2H-benzimidazole 1,3-dioxides, separase inhibitors, by reaction of o-benzoquinone dioximes with ketones. / Chugunova, Elena; Samsonov, Vladimir; Akylbekov, Nurgali et al.
In: Tetrahedron, Vol. 73, No. 27-28, 06.07.2017, p. 3986-3992.Research output: Contribution to journal › Article › peer-review
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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
N1 - Publisher Copyright: © 2017 Elsevier Ltd
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