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31.
An unexpected three-component condensation reaction between an isocyanide, isoquinoline and a strong CH-acid efficiently provides 1,2-dihydroisoquinoline derivatives in a one-pot reaction in water at 70 °C without using any catalyst. 相似文献
32.
Hossein A. Oskooie Majid M. Heravi Khadijeh Bakhtiari Shima Taheri 《Monatshefte für Chemie / Chemical Monthly》2007,138(9):875-877
Summary. A facile synthesis of quinoxaline derivatives catalyzed by KHSO4 in very high yields at room temperature is reported. 相似文献
33.
A novel four-component reaction between 2-formylbenzoic acids, malononitrile, isocyanides, and alcohols has been developed for a highly efficient preparation of alkyl-2-(1-(alkylcarbamoyl)-2,2-dicyanoethyl)benzoate derivatives. This high atom economy reaction led to the construction of two carbon-carbon bonds, one amide, and one ester group in a single synthetic step. Furthermore, a three-component reaction between 2-formylbenzoic acids, malononitrile, and isocyanides in dichloromethane for the preparation of isochromeno[3,4-b]pyrroles has been reported. 相似文献
34.
Ebrahim Abouzari-Lotf Abbas Shockravi Ali Javadi 《Polymer Degradation and Stability》2011,96(5):1022-1028
A series of novel fluorinated heat-resistant poly(amide imide)s (PAIS) based on non-coplanar diimide-diacid monomer (DIDA) were synthesized and characterized. The poly(amide imide)s were obtained in high yields and possessed inherent viscosities in the range of 0.47-0.91 dL g−1. All of the polymers were amorphous in nature, showed outstanding solubility and could be readily soluble in common organic solvents such as N,N-dimethylacetamide, N-methyl-2-pyrrolidinoned, dimethyl sulfoxide, N,N-dimethylformamide, pyridine and tetrahydrofuran. Glass transition temperatures were in the range of 221-263 °C, as determined by differential scanning calorimetry. Degradation temperatures for 10% weight loss occurred all above 520 °C and char yields was more than 50% at 700 °C in nitrogen atmosphere. Moreover, these PAIs possessed low refractive indexes (n = 1.58-1.59), birefringence (Δn = 0.008-0.013), and dielectric constants (? ≈ 2.5) due to the trifluoromethyl pendent groups and ortho-catenated aromatic rings that interrupt chain packing and increase free volume. 相似文献
35.
The comparative electrochemical behavior of self-assembled monolayers of two Schiff's bases, 2-{[(Z)-1-(3-furyl)methylidene]amino}-1-benzenethiol (FMAB) and 2-{[(2-sulfanylphenyl)imino]methyl}phenol (SIMP) on a bare gold electrode (Au FMAB SAM-modified electrode and Au SIMP SAM-modified electrode, respectively), was investigated by means of cyclic voltammetry and electrochemical impedance spectroscopy in a 0.1 mol L(-1) KCl solution that contains 5.0 × 10(-3) mol L(-1) [Fe(CN)(6)](3-/4-). The results revealed that the modified electrodes showed an electrocatalytic activity toward the anodic oxidation of dopamine by a marked enhancement in the current response and lower overpotential (60 and 90 mV for the Au FMAB and Au SIMP SAM-modified electrodes, respectively) in phosphate buffer solution at pH 6.0. The Au SIMP SAM-modified electrode was applied successfully to the determination of dopamine in the presence of a high concentration of ascorbic acid. Selective detection was realized in total elimination of ascorbic acid response-a method different from the ones based on the potential separations. The detection limit of dopamine was 5.0 × 10(-8) mol L(-1) in a linear range from 1.0 × 10(-6) to 1.2 × 10(-4) mol L(-1) in the presence of 1.0 × 10(-3) mol L(-1) ascorbic acid. The interference studies also showed that the Au SIMP SAM-modified electrode exhibited good selectivity in the presence of a large excess of uric acid and could be employed for the determination of dopamine in pharmaceutical formulations, plasma samples and human urine with adequate selectivity and precision. 相似文献
36.
Peter Schiess Charles Monnier Peter Ringele Ebrahim Sendi 《Helvetica chimica acta》1974,57(6):1676-1691
Addition of phenyl-, alkyl-, alkenyl- and alkinyl-Grignard reagents to pyridine-N-oxide in THF leads to 5-substituted (2Z, 4E)-pentadien-aldoximes 6 having (E) (syn)-configuration of the C, N-double bond. The unsaturated oximes are shown to arise through an electrocyclic ring opening reaction from the primary Grignard adducts 5 . These can be trapped by protonation at low temperature. 相似文献
37.
Shahla Mozaffari Marzieh Chaloosi Faten Divsar Ebrahim Abouzari-Lotf Samad T Bavili Ali Yousefi 《Phosphorus, sulfur, and silicon and the related elements》2013,188(10):2439-2448
The complexation reactions between 7,10,13-triaza-1-thia-4,16-dioxa-20,24-dimethyl-2,3;17,18-dibenzo-cyclooctadecane-6,14-dione ( TTD ) and 7,10,13-triaza-1-sulfoxo-4,16-dioxa-20,24-dimethyl-2,3;17,18-dibenzo-cyclooctadecane-6,14-dione ( TSD ) macrocycles with Ag+, Cd2+, Cu2+, Pb2+, Sr2+, Tl+, and Zn2+ ions have been studied in ethanol and methanol solutions at 25°C. The complexes formed between macrocycles ( TTD ) and ( TSD ) with these metals cations had a stiochiometry of 1:1 and 1:2, respectively. The stability constants of the resulting complexes were determined and found to decrease in the order Cu2+ > Zn2+ > Ag+ > Tl+ > Cd2+ > Pb2+ > Sr2+ with macrocycle ( TTD ) and Tl+ > Zn2+ > Cd2+ > Pb2+ > Cu2+ > Ag+ > Sr2+ with macrocycle ( TSD ). 相似文献
38.
Benzo[b][1,4]oxazines have been synthesized in good to excellent yields in the presence of the ionic liquid 1-butyl-3-methylimidazolium bromide [bmim]Br under relatively mild conditions without any added catalyst, The method offers the advantages of good yields and short reaction times, and the ionic liquid can be easily separated from the product and reused. 相似文献
39.
40.
Contamination of therapeutic human immunoglobulin preparations with apolipoprotein H (β2‐glycoprotein I) 下载免费PDF全文
Friedrich Lackner Gerhard Beck Stephanie Eichmeir Manfred Gemeiner Karin Hummel Dieter Pullirsch Ebrahim Razzazi‐Fazeli Alexandra Seifner Ingrid Miller 《Electrophoresis》2014,35(4):515-521
Polyclonal immunoglobulin (Ig) concentrates are important biological medicinal products and the assurance of their quality and safety is crucial. In our present approach we used proteomic methods to check the purity of commercial Ig products of different origin. The experimental setup included nonreducing 2DE or DIGE combined with MALDI‐TOF and the thrombin generation assay, a routine safety test for pharmaceutical Ig preparations, and was complemented by a specific immunoassay. 2DE patterns displayed contaminations with trace amounts of human apolipoprotein H (Apo‐H), transferrin, albumin, and its fragments. In contrast to the latter, Apo‐H is a protein that is active in the coagulation cascade, and thus a potential involvement in thromboembolic events in vivo cannot be excluded. It was found by 2DE and MALDI‐TOF to be a contaminant of several Ig preparations. Spiking experiments of Ig preparations with pure Apo‐H demonstrated an Apo‐H concentration dependent increase in thrombin generation assay values. Traces of Apo‐H are possibly also contributing to unwanted side effects, as already known for factor XIa. The significance of Apo‐H contaminations for these side effects might be verified by detailed analyses of pharmacovigilance data. 相似文献