Halogenation of N-substituted p-quinone monoimines and p-quinone monooxime ethers: XIV. Halogenation of N-[arylsulfonylimino(phenyl)methyl]-2,5-dialkyl-1,4-benzoquinone monoimines and their reduction products

被引：0

作者：

A. P. Avdeenko

S. A. Konovalova

O. P. Ledeneva

A. A. Santalova

V. V. Pirozhenko

G. V. Palamarchuk

O. V. Shishkin

机构：

[1] Donbass State Engineering Academy,Institute of Organic Chemistry

[2] National Academy of Sciences of Ukraine,Institute of Single Crystals

[3] National Academy of Sciences of Ukraine,undefined

[4] Karazin Kharkiv National University,undefined

来源：

Russian Journal of Organic Chemistry | 2012年 / 48卷

关键词：

Aminophenol; Phenylsulfonyl; Quinoid Ring; Quinone Imine; Dimethylphenyl;

D O I：

暂无

中图分类号：

学科分类号：

摘要：

Despite steric hindrances created by the bulky substituent on the nitrogen atom, halogenation of 2,5-dialkyl-N-[arylsulfonylimino(phenyl)methyl]-1,4-benzoquinone monoimines fairly readily gives their derivatives having two halogen atoms in the quinoid ring.

引用

页码：928 / 937

页数：9

共 38 条

[11] Halogenation of N-substituted p-quinone monoimines and p-quinone monooxime ethers: XV. Synthesis and bromination of 4-(cinnamoyloxyimino)-cyclohexa-2,5-dienones
Konovalova, S. A.
Avdeenko, A. P.
Goncharova, S. A.
RUSSIAN JOURNAL OF ORGANIC CHEMISTRY, 2016, 52 (07) : 939 - 945
[12] Halogenation of N-substituted p-quinone imines and p-quinone oxime esters: IV. Chlorination and bromination of N-arylsulfonyl-2(3)-methyl(2-chloro)-1,4-benzoquinone monoimines
A. P. Avdeenko
S. A. Konovalova
Russian Journal of Organic Chemistry, 2006, 42 : 349 - 364
[13] Halogenation of N-substituted p-quinone imines and p-quinone oxime esters:: IV.: Chlorination and bromination of N-arylsulfonyl-2(3)-methyl(2-chloro)-1,4-benzoquinone monoimines
Avdeenko, AP
Konovalova, SA
RUSSIAN JOURNAL OF ORGANIC CHEMISTRY, 2006, 42 (03) : 349 - 364
[14] Halogenation of N-substituted p-quinone monoimines and p-quinone monooxime esrers: XI. Synthesis and halogenation of 4-[aryl(alkyl)aminocarbonyl-oxyimino]cyclohexa-2,5-dien-1-ones
A. P. Avdeenko
S. A. Konovalova
A. G. Sergeeva
Russian Journal of Organic Chemistry, 2010, 46 : 830 - 843
[15] Halogenation of N-substituted p-quinone monoimines and p-quinone monooxime esters: XI. Synthesis and halogenation of 4-[aryl(alkyl)aminocarbonyl-oxyimino]cyclohexa-2,5-dien-1-ones
Avdeenko, A. P.
Konovalova, S. A.
Sergeeva, A. G.
RUSSIAN JOURNAL OF ORGANIC CHEMISTRY, 2010, 46 (06) : 830 - 843
[16] Halogenation of N-substituted p-quinone monoimines and p-quinone monooxime esters: VII. Halogenation of 4-aroyl(arylsulfonyl)imino- and 4-aroyl(arylsulfonyl)-oxyimino-2,6-diisopropylcyclohexa-2,5-dien-1-ones
A. P. Avdeenko
V. V. Pirozhenko
O. V. Shishkin
S. V. Shishkina
S. A. Konovalova
O. N. Ludchenko
Russian Journal of Organic Chemistry, 2008, 44 : 542 - 552
[17] Halogenation of N-substituted p-quinone monoimines and p-quinone monooxime esters:: VII.: Halogenation of 4-aroyl(arylsulfonyl)imino- and 4-aroyl(arylsulfonyl)oxyimino-2,6-diisopropylcyclohexa-2,5-dien-1-ones
Avdeenko, A. P.
Pirozhenko, V. V.
Shishkin, O. V.
Shishkina, S. V.
Konovalova, S. A.
Ludchenko, O. N.
RUSSIAN JOURNAL OF ORGANIC CHEMISTRY, 2008, 44 (04) : 542 - 552
[18] Activated sterically strained C=N bond in N-substituted p-quinone mono- and diimines: XIV. Reaction of some 3,5-dimethyl-1,4-benzoquinone monoimines with alcohols
A. P. Avdeenko
S. A. Konovalova
V. M. Vasil’eva
G. V. Palamarchuk
V. N. Baumer
O. V. Shishkin
Russian Journal of Organic Chemistry, 2013, 49 : 49 - 59
[19] Halogenation of N-substituted p-quinone imines and p-quinone oxime esters:: III.: Regioselectivity in the halogenation of N-aroyl(arylsulfonyl)oxyimino-2,5-cyclohexadienones
Avdeenko, AP
Konovalova, SA
Il'chenko, AY
Glinyanaya, NM
RUSSIAN JOURNAL OF ORGANIC CHEMISTRY, 2006, 42 (01) : 56 - 65
[20] Halogenation of N-substituted p-quinone imines and p-quinone oxime esters: III. Regioselectivity in the halogenation of N-aroyl(arylsulfonyl)oxyimino-2,5-cyclohexadienones
A. P. Avdeenko
S. A. Konovalova
A. Ya. Il’chenko
N. M. Glinyanaya
Russian Journal of Organic Chemistry, 2006, 42 : 56 - 65

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