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991.
M. Zh. Ovakimyan S. K. Barsegyan A. S. Pogosyan N. M. Kikoyan M. G. Indzhikyan 《Russian Journal of General Chemistry》2006,76(11):1757-1759
Dehydrogenation of 1-(diphenylphosphinoyl)-2-hydrazino-substituted ethanes and N-butyl-N′-phenylhydrazine to the corresponding hydrazone derivatives is performed. Both reactions were established to involve predominantly, if not exclusively, an azo intermediate. 相似文献
992.
A. M. Genaev G. E. Sal’nikov V. G. Shubin 《Russian Journal of Organic Chemistry》2007,43(8):1134-1138
By DFT method energy barriers were calculated for carousel rearrangements of bicyclo[3.1.0]hexenyl, cyclobutenyl, and homotropylium cations. A plausible agreement between calculated and experimental findings was found. 相似文献
993.
Devyatkina T. I. Gun'ko Yu. L. Mikhalenko M. G. 《Russian Journal of Applied Chemistry》2001,74(7):1122-1125
The influence exerted by addition of -hydroxynaphthoic acid and combined additive Hg + Pb + -hydroxynaphthoic acid on the corrosion and self-discharge of a porous zinc electrode in alkali solution was studied. 相似文献
994.
Enantioseparations using capillary electromigration techniques in nonaqueous buffers 总被引:3,自引:0,他引:3
This review summarizes recent developments in the field of enantioseparations in capillary electromigration techniques using nonaqueous background electrolytes. The more established and rather intensively reviewed field of nonaqueous chiral capillary electrophoresis (NAQ-CE) is covered in less detail whereas more attention is paid to the relatively new field of nonaqueous capillary electrochromatography (NAQ-CEC). 相似文献
995.
Veliev M. G. Chalabieva A. Z. Shatirova M. I. Akperova E. G. 《Russian Journal of Organic Chemistry》2003,39(6):825-830
Diene condensation of cyclopentadiene with 2-substituted allylacetylenes occurs nonselectively at a double and triple bonds; therewith the dienophile activity grows in parallel with the electron-withdrawing properties of the substituent. Depending on electronic character of functional groups the reaction proceeds as neutral diene synthesis. The relative activity of cyclopentadiene and 1,3-cyclohexadiene in reactions with allylacetylenes is essentially governed by the different distance between the 1,4-reactive sites in these systems. 相似文献
996.
S. L. Bogza K. I. Kobrakov M. Yu. Zubritskii S. Yu. Suikov V. I. Dulenko 《Chemistry of Heterocyclic Compounds》1997,33(1):74-77
Treatment of N-phenyl-2-(1-R-indol-3-yl)succinimides with acetyl perchlorate leads to acylation of the benzene ring of the indole substituent.L. M. Litvinenko Institute of Physico-Organic and Carbon Chemistry, Ukrainian Academy of Sciences, Donetsk 340114. A. N. Kosygin State Textile Academy, Moscow 117918, GSP-1. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 85–88, January, 1997. 相似文献
997.
998.
A carborane-containing stable simple enol — 1-2-isopropyl-o-carboran-I-yl)-1-phenyl2-mesityl-2-lrydroxyctlrylcne — has been synthesized. This enol does not isomerize to the starting ketone or keto-enol mixture even after prolonged heating in benzene in the presence of CF3COOH.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 6, pp. 1561–1563, June, 1996. 相似文献
999.
1,2,2-Trimethyldisilane-1,1,2-triol (1) is formed as an unstable intermediate upon hydrolysis of oligo(trimethyldisilanylsesquiazane). In the absence of trapping
agents it undergoes rapid condensation to give ether-soluble poly(trimethyldisilanyloxane) which contains silanol groups.
Treatment of the hydrolysis products with chlorotrimethylsilane in the presence of triethylamine affords trimethylsiloxy derivatives,
(Me3SiO)2MeSiSiMe2(OSiMe3),5,6, and [Si2Me3O
x
(OSiMe3)
y
]
n
. The isolation of these products indicates that disilanetriol1 readily undergoes condensation to form hydroxylcontaining six-membered rings and polysiloxanes. The condensation of compound1 in the presence of Me3SiOH has been studied. The ratio between the isomeric cyclosiloxanes5 and6 has been determined both by1H NMR spectroscopy and by a chemical method (chlorinolysis).
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 10, pp. 1788–1792, October, 1993. 相似文献
1000.
We have studied the kinetics of the process of epoxidation of 1-octene by tert-butyl hydroperoxide in the presence of molybdenum boride MoB2. We have studied the effect of the concentrations of starting materials and reaction products on the process. We suggest a kinetic scheme and we calculate the kinetic parameters of the process. 相似文献