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991.
Marco Berettoni Giovanna De Chiara Tommaso Iacoangeli Paola Lo Surdo Rinaldo Marini Bettolo Lorenzo Montagnini Di Mirabello Luca Nicolini Rita Scarpelli 《Helvetica chimica acta》1996,79(7):2035-2041
A novel preparation of methyl (13S)-13-hydroxyisoatisiren-18-oate ( 4 ), a key-intermediate in a synthesis of (+)-methyl trachyloban-18-oate ((+)- 1 ), from (?)-abietic acid, is described. Since (?)- 1 has been previously converted into (?)-methyl 16-oxo-17-norkauran-18-oate ((?)- 16 ), our preparation of 4 constitutes also a formal total synthesis, from (?)-abietic acid, of (+)- 16 . Key steps in this approach were the allene photoaddition to podocarp-8(14)-en-13-one ( 5 ) and the conversion of the endo-toluene-4-sulfonate 11 into the exo-benzoate 12b . 相似文献
992.
Lhoëst G Zey T Verbeeck RK Wallemacq P Maton N De Houx JP Latinne D 《Journal of mass spectrometry : JMS》1999,34(1):28-32
It was demonstrated that rapamycin is metabolized in vitro by pig liver microsomes under the influence of the cytochrome P450-dependent mixed function oxygenase system to a rapamycin tris-epoxide metabolite, as demonstrated by electrospray tandem mass spectrometry. The in vitro immunosuppressive activity of this metabolite was found to be lower than that of rapamycin, probably because the rapamycin effector sector was structurally modified. The effector region of rapamycin was recognized to include the conjugated double bonds of this compound and metabolic reactions affecting this region may change the binding affinity of the rapamycin-FKBP binary complex towards another pharmacological receptor bound to the binary complex. Moreover, metabolic modifications in the effector region are probably able to induce a change in the binding affinities of the rapamycin-FKBP binary complex, including the pipecolic acid moiety and the lactone function of the parent drug. 相似文献
993.
Angelo Liguori Loredana Maiuolo Antonio De Nino Antonio Procopio Giovanni Sindona 《Journal of the American Society for Mass Spectrometry》1999,10(10):975-982
Rules for the gas-phase fragmentation mechanism of the negative ions of lipophilic phosphotriester molecules of biological interest have been established by fast-atom bombardment mass spectrometry/mass spectrometry. The mass-analyzed ion kinetic energy spectra of the [M ? H]? of dinucleoside (1–4) and nucleoside glucopyranoside (5–9) phosphotriesters show that in the absence of charges on the phosphate bridge, the availability of acidic protons on the 5′-end nucleobase drives a preferred reaction path which leads to 5′-O-nucleotide or 6-O-glucopyranoside monophosphate anions. 相似文献
994.
Gaetano Guerra Odda Ruiz De Ballesteros Vincenzo Venditto Maurizio Galimberti Franco Sartori Rachele Pucciariello 《Journal of Polymer Science.Polymer Physics》1999,37(11):1095-1103
Structural (X‐ray diffraction), melting (differential scanning calorimetry), as well as mechanical (tensile tests) characterizations on uncrosslinked ethene–propene copolymer samples, obtained using a metallocene‐based catalytic system and having an ethene content in the range 80–50% by mol, are reported. Samples with an ethene content in the range 80–60% by mol present a disordered pseudohexagonal crystalline phase, whose melting moves from ≈ 40°C down to ≈ −20°C as the ethene content is reduced. The dramatic influence of the crystalline phase on tensile properties of uncrosslinked ethene–propene copolymers is shown. In particular, highest elongation at break values are obtained for samples being essentially amorphous in the unstretched state and partially crystallizing under stretching. On the other hand, lowest tension set values (most elastic behavior) are observed for samples presenting, already in the unstretched state, microcrystalline domains acting as physical crosslinks in a prevailing amorphous phase. © 1999 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 37: 1095–1103, 1999 相似文献
995.
Pascale De Meuter Jo Amelrijckx Hubert Rahier Bruno Van Mele 《Journal of Polymer Science.Polymer Physics》1999,37(20):2881-2892
The slow isothermal crystallization of concentrated amorphous starch systems is measured by Modulated Differential Scanning Calorimetry (MDSC). It can be followed continuously by the evolution (stepwise decrease) of the MDSC heat capacity signal (Cp), as confirmed with data from X-ray diffractometry, Dynamic Mechanical Analysis, Raman spectroscopy, and conventional Differential Scanning Calorimetry. Isothermal MDSC measurements enable a systematic study of the slow crystallization process of a concentrated starch system, such as a pregelatinized waxy corn starch with 24 wt % water and 76 wt % starch. After isothermal crystallization, a broad melting endotherm with a bimodal distribution is observed, starting about 10°C beyond the crystallization temperature. The bulk glass transition temperature (Tg) decreases about 15°C during crystallization. The isothermal crystallization rate goes through a maximum as a function of crystallization time. The maximum rate is characterized by the time at the local extreme in the derivative of Cp (tmax), or by the time to reach half the decrease in Cp (t1/2). Both tmax and t1/2 show a bell-shaped curve as a function of crystallization temperature. The temperature of maximum crystallization rate, for the system studied, lies as high as 75°C. This is approximately 65°C above the initial value of Tg. Normalized Cp curves indicate the temperature dependence of the starch crystallization mechanism. © 1999 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 37: 2881–2892, 1999 相似文献
996.
Huan Dong Shu‐Gui Cao Zheng‐Qiang Li Si‐Ping Han De‐Lin You Jia‐Cong Shen 《Journal of polymer science. Part A, Polymer chemistry》1999,37(9):1265-1275
Polymerization of several lactones were carried out by employing Pseudomonas sp. lipase as the catalyst. The data indicate that water is consumed at the onset of polymerization and released in part during subsequent stages, leading us to propose a complex mechanism for the enzymatic polymerization of lactone. This mechanism involves both ring‐opening and linear condensation polymerization. The former was dominant at the early stage while the latter was dominant in the later stage. In addition, the reaction media showed complex influences on enzymatic polymerization. Some organic solvents increased the degree of polymerization (DP) and decreased the molecular weight distribution. A strategy to increase the molecular weight of the polymer is introduced, which led to the synthesis of a polymer with a number‐average molecular weight (Mn) of 14,500—the highest Mn of poly(ε‐caprolactone) prepared by enzyme‐catalyzed polymerization thus far—and molecular weight distribution of 1.23. © 1999 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 37: 1265–1275, 1999 相似文献
997.
Joo Henrique Zimnoch Dos Santos Marcelo Barbosa Da Rosa Cristiano Krug Fernanda Chiarello Stedile Monica Carcuchinski Haag Jairton Dupont Madalena De Camargo Forte 《Journal of polymer science. Part A, Polymer chemistry》1999,37(13):1987-1996
The effects of polymerization conditions were evaluated on the production of polyethylene by silica-supported (n-BuCp)2ZrCl2 grafted under optimized conditions and cocatalyzed by methylaluminoxane (MAO). The Al : Zr molar ratio, reaction temperature, monomer pressure, and the age and concentration of the catalyst were systematically varied. Most reactions were performed in toluene. Hexane, with the addition of triisobutilaluminum (TIBA) to MAO, was also tested as a polymerization solvent for both homogeneous and heterogeneous catalyst systems. Polymerization reactions in hexane showed their highest activities with MAO : TIBA ratios of 3 : 1 and 1 : 1 for the homogeneous and supported systems, respectively. Catalyst activity increased continuously as Al : Zr molar ratios increased from 0 to 2000, and remained constant up to 5000. The highest activity was observed at 333 K. High monomer pressures (≈ 4 atm) appeared to stabilize active species during polymerization, producing polyethylenes with high molecular weight (≈ 3 × 105 g mol−1). Catalyst concentration had no significant effect on polymerization activity or polymer properties. Catalyst aging under inert atmosphere was evaluated over 6 months; a pronounced reduction in catalyst activity [from 20 to 13 × 105 g PE (mol Zr h)−1] was observed only after the first two days following preparation. © 1999 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 37: 1987–1996, 1999 相似文献
998.
A very stable chelating resin was prepared by adsorption of (o-[3,6-disulfo-2-hidroxy-1-naphthylazo]-benzenearsonic acid) (thorin) on a macroporous resin Amberlite XAD-7. The optimal conditions for preparing it were obtained through the study of the adsorption properties of the resin and the thermodynamic quantities of the adsorption processes. Likewise, the behavior of the loaded resin with the rare earth elements (REE) were studied (pH of retention, sorption kinetics, etc). The conditions to prepare a thin film with this system were also evaluated. The loaded resin was successfully used for the separation and preconcentration of Sm(III), Eu(III) and Gd(III) prior to their determination by X-ray fluorescence (XRF) spectrometry. The preconcentration factor obtained was 500 and the concentrations at low detection limit were 13.8, 17 and 15.7 microg l(-1) for Sm, Eu and Gd, respectively. 相似文献
999.
建立了加速溶剂萃取/气相色谱-三重四极杆串联质谱(ASE/GC-MS/MS)同时测定纺织品中24种多环芳烃(PAHs)的方法。样品经丙酮加速溶剂萃取,旋蒸浓缩后采用DB-35色谱柱程序升温分离,选择多反应监测模式(MRM)采集,外标法定量。结果表明,在一定浓度范围内多环芳烃的峰面积与质量浓度呈良好的线性关系,相关系数(r~2)均大于0.994,方法检出限为0.000 3~0.03 mg/kg,方法定量下限为0.001~0.10 mg/kg,加标回收率为80.3%~103%,相对标准偏差(RSD)为1.3%~9.2%。该方法灵敏、准确可靠,能满足纺织品中24种多环芳烃的测试要求。 相似文献
1000.
Ricardo A. Luna-Mora Ángeles Torres-Reyes Oscar A. González-Cruz Fernando Ortega-Jiménez Hulme Ríos-Guerra Jessica V. González-Carrillo 《Green Chemistry Letters and Reviews》2018,11(4):371-378
The efficiency of conventional heating energy source compared with Infrared (IR), Ultrasound (US), Microwave and the simultaneous combination US–IR eco-friendly approaches for preparation of new N-(5-R1 -amino-2-nitrophenyl)acetamides and 5-R1-amino-2-nitroaniline by Nucleophilic Aromatic Substitution (SNAr) via addition–elimination reactions on the halogens F, Cl, Br, I, employing amines as nucleophiles were explored. Moreover, phenyldiazenyl derivatives in good yields by an oxidative one-pot SNAr-based amination reaction from an unusual oxidation of 2-phenylhydrazinyl derivatives in DMSO was prepared. 相似文献