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851.
The reaction of imidazole with benzoyl chloride in pyridine affordedcis-1,2-bis(benzoyl-amino)ethylene (1) rather than 2-benzoylimidazole, as has been suggested previously. The structure of1 was confirmed by1H NMR spectroscopy and X-ray diffraction study.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 8, pp. 1593–1595, August, 1998. 相似文献
852.
The reactions of aliphatic β-amino-β-trifluoromethylvinyl ketones with an excess of ethylenediamine at room temperature afforded
the corresponding 2,3-dihydro-1H-1,4-diazepines or substituted 2-acetonyl-2-trifluoromethylimidazolidines (the latter were obtained when the approach to the
carbonyl group was sterically hindered).
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 11, pp. 2305–2308, November, 1998. 相似文献
853.
N. E. Golantsov A. V. Karchava M. A. Yurovskaya 《Chemistry of Heterocyclic Compounds》2006,42(8):1021-1024
Methods of obtaining ketones and enamino esters have been developed on the basis of reactions of 1-(1-phenylethyl)indole-2-carbonitrile
with organomagnesium and organozinc compounds. Removal of a benzyl group from the indole nitrogen atom by the Grignard reagent
has been discovered.
__________
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1179–1183, August, 2006. 相似文献
854.
Marialuisa Russo Gabriella Poggi Maria Luisa Navacchia Mila D'Angelantonio Salvatore S Emmi 《Research on Chemical Intermediates》2006,32(2):153-170
Chemical radiolytic oxidation induced by OH addition on 1-(2-furan-2-yl-5-hydroxy-6-hydroxymethyl-[1,3]dioxan-4-yl)-ethan-1,2-diol
(sorbitylfurfural, SF) leads, in the presence of controlled amounts of oxygen, to a permanent functional modification of the
target molecule. The yield of conversion reaches 60% of the starting material. LC-MS analysis allowed the identification,
as final products, of carboxylic acids, butenal and hydroxy-furan derivatives in which the sugar chain remains unbroken, while
the furanic ring is attacked first by OH and then by oxygen, giving in succession an intra-/inter-molecular rearrangement
of the allylperoxyl radicals thus formed. The proposed oxidation of the furanic ring envisages the peroxyl intermediates undergoing
mono- and/or bi-molecular reactions; a reaction path has been outlined and is reported here. The presence of unsaturated bonds
in the final products could provide a further site for radical scavenger activity. Therefore, the fast reaction with O2 and the rearrangement of the produced peroxyl radicals to species, which are likely to be effective OH-capturers, reinforces
the antioxidant ability of SF. 相似文献
855.
Various carboxamides are synthesized from the corresponding carboxylic acids and amines with high product-selectivities using 2-methyl-6-nitrobenzoic or 2,4,6-trichlorobenzoic anhydride in the presence of 4-(dimethylamino)pyridine. 相似文献
856.
Comparison between adsorption isotherm determination techniques and overloaded band profiles on four batches of monolithic columns 总被引:1,自引:0,他引:1
The adsorption isotherms of 4-tert.-butyl phenol were measured on four different monolithic columns, using three different techniques, classical frontal analysis (FA), the perturbation on a plateau method (PP) and the recently introduced numerical procedure known as the inverse numerical method (IN). This last approach requires only the recording of a few overloaded profiles and has the potential advantage of affording a dramatic decrease of the amounts of compounds, solvent, and time needed to determine accurate estimates of the coefficients of the isotherm. The reproducibility of the adsorption data measured on the four columns is discussed with reference to the specific techniques used for obtaining these data and to the most suitable equation used for modeling them. The data obtained for the different columns were highly consistent. The inverse numerical approach was confirmed to provide a powerful, accurate, and economic method for measuring single component adsorption data. 相似文献
857.
858.
在仔细研辉光放电光源工作过程的基础上,在国内首先设计、制成了HGZ-Ⅱ型自动辉光放电光源。该光源除换样品外,实现了抽空、进气、对光、预燃、曝光、充气、复位等摄谱全过程的自动控制。有水压、真空度、短路保护措施和醒铃线路。设计合理,性能良好,操作简便,工作安全,可靠。程控部分的编排包括顺序控制。时序控制和条件控制。由于使用了通用执行元、器件,降低了成本,提高了耐用性。为满足表层,逐层分析的需要,还专门设计了计数电路。供电源实现了高压直流供电和脉冲供电。该光源可应用于合金中主成分和少量杂质分析及金属、合金表层,逐层成分分析。 相似文献
859.
M. J. van Bommel P. M. C. ten Wolde T. N. M. Bernards 《Journal of Sol-Gel Science and Technology》1994,2(1-3):167-170
The influence of MPS on the hydrolysis and condensation process of TEOS is studied by means of hydrolysis time (t
H) and gelation time (t
G) curves. The addition of MPS to a mixture of TEOS, ethanol and water results in a substantial increase in t
G. The increase is most pronounced when adding takes place in the acid step of the sol-gel process of TEOS.In acid environment hydrolysis of MPS will be dominant compared to hydrolysis of TEOS. This results in an effective decrease of the amount of water available for the hydrolysis of TEOS. However, this decrease in water concentration cannot explain the complete effect of the addition of MPS. The hydrolysed MPS will also be incorporated in the gel network and will strongly influence the cross-linking ability. The lesser functionality of MPS compared to TEOS and the steric hindrance of the acrylate group results in a large increase in t
G. 相似文献
860.
The initial formation of organotin derivatives with Sn-S-N bonds in heterolytic reactions of hexamethylditin or trimethyltin sulfide withN-(chlorothio)phthalimide is suggested. Subsequent interaction of these compounds with sulfenyl chloride affordsN, N-thioorN, N-dithiobisphthalimide. Homolytic reaction of hexamethylditin withN, N-dithiobisphthalimide also occursvia an organotin intermediate, which, in the absence of a nucleophilic reagent, eliminates sulfur and converts intoN-trimethylstannylphthalimide.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 12, pp. 2111–2114, December, 1993. 相似文献