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11.
α-乙酰基二硫缩烯酮α碳原子的酰化反应 总被引:1,自引:0,他引:1
进行了α-乙酰基二硫缩烯酮与酰氯的酰化反应. 以干燥的二氯甲烷为溶剂, 在四氯化钛催化下, α-乙酰基环二硫缩烯酮(1)可与脂肪及芳酰氯(2)反应, 在化合物1的α-碳原子上发生酰化反应, 以较高的产率生成各种α-乙酰基-α-酰基二硫缩烯酮(3). 相似文献
12.
A. V. Kolotaev L. I. Belen’kii A. S. Kononikhin M. M. Krayushkin 《Russian Chemical Bulletin》2006,55(5):892-897
Symmetrical and unsymmetrical α-diketones of the indole series were synthesized by the Friedel-Crafts reaction of 3-indolylglyoxyl
chlorides with heterocycles. A nonconventional reaction of N-unsubstituted diketones with hydrazine producing 3H-pyrazolo[3,4-c]quinoline derivatives was found.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 5, pp. 862–866, May, 2006. 相似文献
13.
Alwyn G. Davies Rajaveen Sivasubramaniam 《Journal of organometallic chemistry》2006,691(16):3556-3561
The thermolysis of the butyltin chlorides at 200-300 °C in the liquid phase has been investigated by 1H, 13C, and 119Sn NMR spectroscopy. The stabilities follow the order: Bu2SnCl2 > Bu3SnCl > BuSnCl3. Only tributyltin chloride showed any evidence of redistribution, giving dibutyltin dichloride, together with metallic tin, butane, and but-1-ene, which would be formed by decomposition of tetrabutyltin. Dibutyltin dichloride decomposed to give mainly butane with no other apparent liquid organotin compound. Butyltin trichloride gave butane, some butene, and metallic tin, and showed no evidence of forming tributyltin chloride by the redistribution reaction, which would have environmental implications for its use in the CVD coating of glass. 相似文献
14.
Proof of Existence and Thermochemical Characterization of the Gaseous Molecule VOCl2 By use of the Knudsen-cell mass spectrometry the existence of VOCl2(g). is proven. Lines of fragmentation are set up for VOCl3(g). The vapor above V2O3(s) with Cl2(g) is examined. The sublimation of VOCl2 is measured at a temperature of 550–620 K. By 2nd law calculations the heat of sublimation is defined. The calculation for the gaseous VOCl2 leads to ΔBH°(VCl2(g), 298 K) = ?(130,4 ± 1,5) kcal · mol?1. The influence of VOCl2(g) for chemical vapor transport reactions of vanadium oxides with Cl2 is discussed by equilibrium calculations. 相似文献
15.
Krasnov V. P. Levit G. L. Korolyova M. A. Bukrina I. M. Sadretdinova L. Sh. Andreeva I. N. Charushin V. N. Chupakhin O. N. 《Russian Chemical Bulletin》2004,53(6):1253-1256
The influence of the reaction conditions (solvent, base) on the diastereoselectivity of acylation of (±)-3-methyl-2,3-dihydro-4H-1,4-benzoxazine with (S)-naproxen and N-tosyl-(S)-proline chlorides was studied. The highest diastereoselectivity was observed for the reaction carried out in benzene in the presence of aliphatic tertiary amines. 相似文献
16.
Application of acetonitrile as a solvent in the catalytic carbonylation of potassiumN,2-dichlorobenzenesulfonamidate allowed to reduce the catalyst/substrate ratio and the CO pressure as compared to those used
with chlorinated hydrocarbons. 相似文献
17.
Sizov A. I. Zvukova T. M. Belsky V. K. Bulychev B. M. 《Russian Chemical Bulletin》2001,50(11):2200-2202
The heterometallic zirconocene(iii) aluminum hydride complex (Cp2ZrH)2HAlCl2·C4H8O2·C6H6 was synthesized by reduction of Cp2ZrCl2 with lithium aluminum hydride in the presence of Cp2TiBH4 and 1,4-dioxane, and its structure was established by X-ray diffraction analysis. 相似文献
18.
The solid-liquid equilibrium diagrams of binary mixtures involving magnesium nitrate hexahydrate with cobalt nitrate hexahydrate, nickel nitrate hexahydrate (partly), manganese nitrate tetrahydrate, and iron(III) nitrate nonahydrate and of magnesium chloride hexahydrate with cobalt and nickel chlorides hexahydrates and manganese chloride tetrahydrate, and the of two manganese salts were determined. Those diagrams that showed a simple eutectic were fitted by the Ott equation and where the required BET parameters were available, the magnesium salt rich parts of the liquidus were modeled by means of this method. 相似文献
19.
P. I. Dem'yanov E. M. Myshakin D. P. Krut'ko V. S. Petrosyan 《Russian Chemical Bulletin》1997,46(12):1996-2005
The results of calculations for benzyl chlorides and benzyl bromides that contain substituents in the ring by different quantum-chemical
methods are compared. The electron density on the benzyl carbon atom increases as the electron-withdrawing properties of substituents
are enhanced due to the shift of the electron density from the benzyl halogen atom to the adjacent carbon atom. A topological
analysis according to Bader confirmed the main reason for the change in the paramagnetic shielding of the benzyl13C nuclei. The results of calculations provide, for the first time, an explanation for the resonance upfield13C shift of this atom as the Hammett constant of a substituent increases in compounds of the series under consideration.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 12, pp. 2111–2119, December, 1997. 相似文献
20.
The reaction scope of trifluoromethanesulfonyl azide in diazo transfer reactions was extended to include the preparation of α-cyano-α-diazo-carbonyls, phenyl sulfonyl diazoacetophenone and diethyl diazomalonate in high yields. The effect of the bases used in the diazo transfer reactions were found to have a dramatic influence on the success of the reaction with pyridine being the base of choice. 相似文献