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101.
Monitoring of estradiol and its metabolites in biological samples is essential for the accurate diagnosis of a number of endocrine diseases. In this study, a sensitive, precise and specific GC–MS/MS method for the quantification of 17β-estradiol (17-BE) and its main metabolite, 2-methoxyestradiol (2-MEOE), in plasma was developed and validated. Plasma concentrations of these steroids are currently investigated as diagnostic markers for pre-eclampsia, a systematic disorder of pregnancy and a leading cause of maternal and fetal morbidity and mortality worldwide. 相似文献
102.
Yo Hiranoi Miho Hatanaka Koji Nakano 《Journal of polymer science. Part A, Polymer chemistry》2017,55(13):2150-2159
Di‐ and trinuclear cobalt (Co)–salen complexes with a benzene ring as a rigid linker were explored for epoxide polymerizations. The dinuclear Co–salen complex with a 1,2‐phenylene linker showed higher catalytic activity than the dinuclear Co–salen complex with a 1,3‐phenylene linker and the trinuclear Co–salen complex with a 1,3,5‐benzenetriyl linker for the copolymerization of propylene oxide (PO) with carbon dioxide. A combination of the absolute configuration of the two Co–salen moieties was found to affect its catalytic activity. The optimized dinuclear Co–salen complex with a heterochiral combination demonstrated highest activity and maintained its catalytic activity under a low catalyst concentration. The heterochiral dinuclear Co–salen complex also showed high activity for the copolymerization of PO with cyclic anhydride. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017 , 55, 2150–2159 相似文献
103.
A novel approach to the synthesis of 4-phenylethynylphthalic anhydride has been described.The target compound was synthesized by Pd/Cu catalyzed Sonogashira coupling reaction between phenylacetylene and 4-bromophthalic acid which was for the first time employed as start material,followed by dehydration of 4-phenylethynylphthalic acid.Compared with traditional synthetic routes,this method provides several advantages such as readily available raw materials,convenient manipulation and high yield.The product... 相似文献
104.
SUI XinCe SHI Yan & FU ZhiFeng State Key Laboratory of Chemical Resource Engineering Beijing University of Chemical Technology Beijing China 《中国科学B辑(英文版)》2011,(3)
A novel copolymer network with acetal structure was prepared using bis[4-(vinyloxy)butyl](4-methyl-1,3-phenylene)biscarbamate(BECT)as the crosslinking agent.Firstly,a tri-copolymer of maleic anhydride(MAn),n-butyl vinyl ether(BVE)and 4-hydroxybutyl vinyl ether(HBVE)was synthesized via free-radical polymerization with 2,2′-azobisisobutyronitrile as the initiator.The tri-copolymer consisted of two sorts of alternating units,MAn-alt-BVE and MAn-alt-HBVE.The linear copolymer Poly((MAn-alt-BVE)-co-(MAn-alt-HBVE)... 相似文献
105.
John Kallikat Augustine Rajesha KumarAgnes Bombrun Ashis Baran Mandal 《Tetrahedron letters》2011,52(10):1074-1077
An efficient method for the Beckmann rearrangement of ketoximes to amides mediated by a catalytic amount (15 mol %) of propylphosphonic anhydride (T3P®) is described. Aldoximes underwent second order Beckmann rearrangement to provide the corresponding nitriles in excellent yields on reacting with T3P (15 mol %) at room temperature. The main advantages of this environmentally friendly protocol include procedural simplicity, and particularly ease of isolation of the products. 相似文献
106.
Dimitri D.J. Rousseaux Xavier Drooghaag Pierre Godard Jacqueline Marchand-Brynaert 《Polymer Degradation and Stability》2010,95(3):363-3521
Polypropylene ionic thermoplastic elastomers have been prepared by melt radical grafting of maleic anhydride onto polypropylene in the presence of N-bromosuccinimide followed by neutralization of the resulting elastomeric grafted polypropylene using sodium salts. Sodium hydroxide and sodium acetate were compared in aqueous solution, as anhydrous or hydrated powders. The neutralization reaction was followed by Fourier transform infrared spectroscopy, allowing the development of a method to determine the effective neutralization degree. Important physical changes were recorded upon neutralization. Especially thermal stability, shear storage modulus and complex viscosity in the flow region were largely increased as a function of the neutralization degree. 相似文献
107.
Bangben Yao 《Tetrahedron letters》2008,49(37):5385-5388
In the presence of triflic anhydride, sulfonylation of arenes with sulfonamides proceeded smoothly in Cl2CHCHCl2 at 80-140 °C, which gave rise to the desired products in good to excellent yields. 相似文献
108.
109.
A series of lanthanide coordination polymers, [LnIII(mal)(ox)0.5(H2O)2]·2H2O (Ln = Pr ( 1 ), Nd ( 2 ), and La ( 3 ); H2mal= maleic acid; H2ox = oxalic acid), were synthesized firstly by the reaction of LnIII nitrate salts with maleic anhydrid and oxalic acid under hydrothermal conditions and were characterized by elemental analysis, IR spectroscopy, and single‐crystal X‐ray diffraction. X‐ray diffraction analyses reveal that they are crystallized in orthorhombic space group Fddd. Lanthanide metal center atom (Ln) and its corresponding centrosymmtric atom link through two chelating/bridging bidentate carboxyl groups of maleic acid ligands to form an infinite inorganic rod‐shaped building unit. These rod‐shaped building units were linked to each other through the carbon atoms of the maleate anions on the [110] plane to form lanthanide‐maleic acid layers. The oxalic acid pillared lanthanide‐maleic acid layers with intersected channels by free water molecules consist of a 3D framework structure. The thermogravimetric analyses of 1 – 3 were discussed in detail. The courses of the thermal decomposition of complexes are similar. 相似文献
110.
A new method for constructing the polycyclic skeleton of psiguadial B (1), a meroterpenoid isolated from an evergreen shrub of Myrtaceae, was developed. The terpenoid substructure of 1 was constructed on the basis of a cascade double cyclization reaction of an alkyne dicobalt complex, which afforded the bicyclo[4.3.1]decane derivative having a benzyl group with the correct configuration. The substituted aromatic ring was introduced to the bridgehead position of the intermediate, and bromination under radical conditions followed by intramolecular cyclization reaction resulted in formation of the benzopyran moiety in a stereoselective manner. 相似文献