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991.
Zheng Li Jin-Lan Yu Sheng-Yi Shi Wei Zhu 《Phosphorus, sulfur, and silicon and the related elements》2013,188(5):1031-1037
A rapid method to N-acyl ureas from corresponding N-acyl thioureas is described. N-coumaroyl-N′-arylthioureas, which are easily prepared by the reaction of coumarin-3-carboxylic acid chloride with potassium thiocyanate and arylamines, can be expeditiously transformed into corresponding N-acyl ureas via r.t. grinding with wet silica supported potassium permanganate under solvent-free conditions in an excellent yield. 相似文献
992.
The Reaction Activity of Aromatic Carbonyl Compounds with Diphenylphosphine Oxide Studied by 31P NMR
Jinyun Zheng Xiangming Feng Yujian Yu Xiaomin Zhen Yufen Zhao 《Phosphorus, sulfur, and silicon and the related elements》2013,188(8):1080-1087
Abstract A series of α-hydroxyphosphine oxides were prepared by the reactions of diphenylphosphine oxide and aromatic carbonyl compounds and characterized by 1H NMR, 13C NMR, 31P NMR, FT-IR, ESI-MS, and HR-MS spectra. The reaction rates and experimental conditions of aromatic aldehydes and aromatic ketones were obviously different due to the activity of their carbonyls. The different substituents of the aromatic aldehydes affected the reaction rate too, and the quantitative reactivity of their substituent conformed to the Hammett equation. The results were confirmed by 31P NMR spectroscopy. 相似文献
993.
Jinyun Zheng Yujian Yu Xiaomin Zhen Erbing Yang Yufen Zhao 《Phosphorus, sulfur, and silicon and the related elements》2013,188(11):1564-1575
Abstract A series of new nitrogen heterocyclic compounds containing sulfur–ether (8a–8f) and Schiff-base (9a–9q) functionalities were synthesized by the reaction of the pharmaceutical lead compound containing both benzimidazole and 1,2,4-triazole rings. The compounds were characterized by 1H NMR, 13C NMR, FT-IR, HR-MS, and ESI-MS. 相似文献
994.
Wenyu Tian Chun Li Xiaoyu Liu Luhua Wang Zhong Zheng Xiangyun Wang Chunli Liu 《Journal of Radioanalytical and Nuclear Chemistry》2013,295(2):1423-1430
The diffusion of 125I? in compacted Gaomiaozi (GMZ) bentonite was investigated by capillary in-diffusion method. Apparent and effective diffusion coefficients and accessible porosity of iodide in GMZ bentonite were obtained, and the effect of ionic strength on diffusion parameters was studied. The apparent diffusion coefficients of iodide in compacted GMZ bentonite are in the range of 1.0–6.0 × 10?10 m2 s?1 under the conditions of dry bulk density 1,500 kg m?3 and temperature 298 K, and increase with increasing ionic strength. This effect was explained through the analysis of microscopic structure of compacted bentonite. The iodide can only diffuse in unbound interparticle pore solution of compacted bentonite. The apparent diffusion coefficient is a function of accessible porosity which is decided by the thickness of diffusion double layer, and the thickness is in turn controlled by ionic strength. 相似文献
995.
T. Chen C. Li X. Y. Liu L. H. Wang Z. Zheng X. Y. Wang C. L. Liu 《Journal of Radioanalytical and Nuclear Chemistry》2013,298(1):219-225
The fate and migration behavior of radionuclides in environment are influenced by a series of physical and chemical processes such as advection, hydrodynamic dispersion (including mechanical dispersion and molecular diffusion), retention, chemical reaction and so on. In this study, the migration of 125I? in Beishan granite and the potential retention of iodine by silver halide additives were investigated by a pulse injection column method. All breakthrough curves were analyzed according to the analytical solution of transport equation and the dispersion coefficient (D), and first-order sorption constant (k) were obtained. For conservative nuclide, the dispersion behavior is only related to the dispersion medium. Silver halides were proved having sorption ability for 125I? in the order of AgCl > AgBr > AgI. The transport of iodine in the crushed granite column can be adequately described by the advection–dispersion equation with a first-order, irreversible sorption term. The pulse injection column method can be used as a fast method to evaluate the sorption or retention ability of solid phase. 相似文献
996.
997.
Under solid-liquid PTC conditions, treatment of 1-nitro-4-(4-nitrophenylsulfonyl-methyl)benzene(1) with α,β -unsaturated esters (2a-h) at 35–75°C gave tandem addition-rearrangement products(3a-h). While at higher temperature(75°C), addition-rearrangement-addition products (4a-b) were obtained when acrylates were used. Finally a possible mechanism is proposed. 相似文献
998.
The Vilsmeier reaction of nickel(II) chlorin P6 trimethyl ester with 3-dimethyl-aminoacrolein yielded nickel(II) chlorin P6 20-(2-formylvinyl) trimethyl ester and nickel(II) chlorin P6 3-(1-hydroxyethyl)-3-devinyl-20-(2-formylvinyl) trimethyl ester. Also, the outgrowths of nickel(II) chlorin P6 20-(2-formyl) trimethyl ester and nickel(II) chlorin P6 3-(2-formylvinyl)-3-devinyl-20-(2-formyl) trimethyl ester were obtained by Vilsmeier reaction with dimethylformamide. By treating the derivatives of nickel(II) 20-(2-formyl)-chlorin and nickel(II) 3-(2-formylvinyl)-20-(2-formyl)-chlorin with trifluoracetic acid, the removal of the central nickel(II) ion was accomplished. The derivatives of 20-(2-formyl)-chlorin and 3-(2-formylvinyl)-20-(2-formyl)-chlorin demonstrated considerable bathochromic shift of the major absorption band in the red region of the optical spectrum. 相似文献
999.
Abstract Cefpirome was synthesized in 37.7% overall yield from 3-chloromethyl-7-phenylacetylamino cephalosporanic acid p-methoxybenzyl ester (GCLE) by sequential substitution of C-3 chloride with iodide and 2,3-cyclopentenopyridine, followed by a one-pot procedure including deprotection of carboxyl group, hydrolysis of 7-phenylacetamido, and reaction with 2-mercaptobenzothiazolyl-(Z)-2-(2-aminothiazol-4-yl)-2-methoxyiminoacetate (MAEM). The reaction conditions were as follows: obtained from GCLE at low temperature (?5 to 0 °C) and absence of light, 3-iodomethyl-7-phenylacetylamino cephalosporanic acid p-methoxybenzyl ester (GILE) without purification was reacted directly with 2,3-cyclopentenopyridine, in which the molar ratio of GCLE, NaI, and 2,3-cyclopentenopyridine was 1:2:4, and the molar ratio of the resulting compound p-methoxybenzyl 7-phenylacetylamido-3-(2,3-cyclopenteno-1-pyridinio)methyl-3-cephem-4-carboxylate iodide and MAEM was 1:1.1. The structure of the intermediate and the target compound obtained were determined by nuclear magnetic resonance spectra and mass spectroscopy. 相似文献
1000.
PdCl2(PCy3)2-catalyzed cyclocarbonylative coupling of ortho-chloro arylketimines with CO has been investigated to develop an efficient method for the synthesis of isoindolin-1-ones. The developed synthetic method has the advantages of having easily available starting materials, high atom-economy, and high selectivity. 相似文献