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排序方式: 共有198条查询结果,搜索用时 15 毫秒
1.
2.
Vincenzo Santagada Ferdinando FiorinoElisa Perissutti Beatrice SeverinoSara Terracciano Giuseppe CirinoGiuseppe Caliendo 《Tetrahedron letters》2003,44(6):1145-1148
A novel and convenient microwave-assisted dimerization of an active peptide compound using the DKPs as scaffold is described. The key reaction giving rise to the diketopiperazine scaffold is the intermolecular coupling. No epimerization was detected in the reactions used. Conventional and microwave heating of the reactions are compared. Synthesis by microwave irradiation gave the desired compounds in higher yields and in shorter reaction times than those obtained by conventional heating. 相似文献
3.
A. Cavallini B. Fraboni W. Dusi N. Auricchio M. Zanarini P. Chirco 《Applied Physics A: Materials Science & Processing》2002,75(3):427-429
The time recovery of the spectroscopic capabilities of CdZnTe and CdTe detectors, irradiated with increasing doses of high-
and low-energy neutrons, as well as electrons, has been investigated by studying their spectroscopic behavior at different
photon energies using leakage current measurements and PICTS (photo-induced current transient spectroscopy) analysis. The
detectors were stored at room temperature for up to one year to study the time evolution of their spectroscopic performance
and to correlate it with the presence of defective states in the material. We have observed a clear improvement in the material’s
detection properties with time, though only in those detectors which have not been severely degraded by the irradiation. The
recovery can be associated with a decrease in the concentration of some defective states, thus allowing the assessment of
the crucial role these play in determining the charge collection processes in the material and its spectroscopic capabilities.
Received: 1 August 2001 / Accepted: 3 August 2001 / Published online: 20 December 2001 相似文献
4.
Cyclization of suitable enamino ketones can produce hydroxyphthalides. 相似文献
5.
6.
Antonio Selva Sergio Auricchio Ada M. Truscello 《Journal of mass spectrometry : JMS》1994,29(5):232-237
On electron impact (EI) ionization, two cis/trans pairs of 4-methyl-5-phenyl and 4-phenyl-5-methyl regioisomeric 3-carbethoxy-2-isoxazolines showed normal mass spectra and mass-analysed ion kinetic energy (MIKE) spectra of metastable (MI) and collision-activated (CA) molecule ions, allowing unequivocal differentiation of the regioisomers. The cis/trans stereoisomers of each regioisomer showed very similar normal mass spectra. Very interestingly, the cis- and trans-4-phenyl-5-methyl stereoisomers appeared reasonably differentiated by the molecule ion MIKE spectra, whereas the 4-methyl-5-phenyl regioisomeric pair of stereoisomers did not. The influence of the phenyl substituent to the fragmentation processes was notable. Some fragments of interest were studied by comparison of their MIKE spectra with those of model ions, generated by EI from suitable substrates, including (i) the isomeric α,β-unsaturated oxime, namely ethyl (Z)-2-(hydroxymino)-3-methyl-4-phenylbut-3-enoate, a by-product of importance for the mechanism(s) of the addition/cycloaddition reactions of nitrile oxides to alkenes and (ii) trans-β-methylstyrene, a dipolarophilic reactant in the same reactions. The favoured heterocyclic C(5)–O(1) bond cleavage occurred only for the ionized 4-methyl-5-phenyl 2-isoxazoline pair, leading to a distonic ion of relevance, as it can represent either a reasonable precursor for both the isomerization to the ionized α,β-unsaturated oxime and the EI-induced cycloreversion yielding ionized β-methylstyrene, or the ionized form of a zwitterionic intermediate, which had been proposed previously for the addition/cycloaddition mechanism(s) in the solution phase, currently under study. 相似文献
7.
Amantini D Fringuelli F Piermatti O Pizzo F Vaccaro L 《The Journal of organic chemistry》2003,68(24):9263-9268
The [4 + 2] cycloadditions of 3-nitrocoumarin (1a), 6-chloro-3-nitrocoumarin (1b), and 6-, 7-, and 8-hydroxy-3-nitrocoumarins (1c, 5, and 6) with (E)-piperylene (7), isoprene (8), 2,3-dimethyl-1,3-butadiene (9), 2-methoxy-1,3-butadiene (10), 2,3-dimethoxy-1,3-butadiene (11), and cyclopentadiene (12) were investigated in aqueous medium, in organic solvent and under solventless conditions. The reactions performed in water occurred in heterogeneous phase but were faster than those executed in toluene or dichloroethane (DCE). 1a-c, 5, and 6 behaved as 2pi components in the Diels-Alder cycloadditions with 7-10 and 12, and exo adducts were preferentially or exclusively produced. Surprisingly 1a, behaved as a 4pi component in the cycloaddition in water with 11 and 4-substituted 3-nitrochromanones 20 and 21 were isolated. The cycloadditions of hydroxy-3-nitrocoumarins 1c, 5, and 6 with 1,3-diene 9 did not work in water or in organic solvent, but did work under solventless conditions. Nitrotetrahydrobenzo[c]chromenones 13-16, 24, and 25, originating from the normal electron-demand Diels-Alder reactions, were converted into dihydrodibenzo[b,d]furans 27-31 in water, via one-pot Nef-cyclodehydration reactions. 相似文献
8.
Gino Morisi Marina Patriarca Ferdinando Chiodo Anna Minoprio Antonio Menditto 《Mikrochimica acta》1996,123(1-4):281-290
Between 1992 and 1994, a new screening campaign for blood Pb monitoring in the Italian general population was carried out. Since the first campaign (started in 1978, in accomplishment of the European Community Directive 77/312/EEC) a working group of the Laboratory of Clinical Biochemistry at the Italian National Institute of Health (Istituto Superiore di Sanità), as the Reference Centre (RC), has coordinated the activity of various laboratories spread over the national territory. Appropriate quality assurance procedures, including an external quality assessment scheme (EQAS), were elaborated. Within the EQAS, three or four trials were carried out every year. Each laboratory participating in the trial analyzed eight control samples prepared from cow blood at different Pb concentrations. The results obtained by each peripheral laboratory and the RC between 1992 and 1994 have been compared by regression analysis. The same statistical method was adopted to compare the results obtained by each peripheral laboratory and the RC in the duplicate analysis of about 10 per cent of the human samples collected during the 1992–1994 monitoring campaign. There was no evidence of systematic differences between the regression lines obtained on control and human samples. In spite of the lower Pb concentration in the control samples analyzed during the 1992–1994 campaign, the analytical performance of the laboratories was better than that obtained in the previous screening campaign (1985–1986). Blood Pb levels observed in human samples collected between 1992 and 1994, confirm the downward time trend observed in the campaigns carried out in 1978–1979, 1980–1981 and 1985–1986. This study confirms that the results obtained in an EQAS are representative of the actual performance in the analysis of real (human) samples. 相似文献
9.
Amantini D Beleggia R Fringuelli F Pizzo F Vaccaro L 《The Journal of organic chemistry》2004,69(8):2896-2898
Tetrabutylammonium fluoride (TBAF) is an efficient catalyst in the [3 + 2] cycloaddition reaction of organic nitriles 1 with trimethylsilyl azide (TMSN(3)) in solventless conditions. The corresponding 5-substituted 1H-tetrazoles 2 were obtained under mild conditions and in 80-97% yields. 相似文献
10.
Rosa Sparaco Ewa Kdzierska Agnieszka A. Kaczor Anna Bielenica Elisa Magli Beatrice Severino Angela Corvino Ewa Gibua-Tarowska Jolanta H. Kotliska Giorgia Andreozzi Paolo Luciano Elisa Perissutti Francesco Frecentese Marcello Casertano Anna Leniak Magdalena Bujalska-Zadrony Magorzata Ozibo Raffaele Capasso Vincenzo Santagada Giuseppe Caliendo Ferdinando Fiorino 《Molecules (Basel, Switzerland)》2022,27(19)
A new series of 5-norbornene-2-carboxamide derivatives was prepared and their affinities to the 5-HT1A, 5-HT2A, and 5-HT2C receptors were evaluated and compared to a previously synthesized series of derivatives characterized by exo-N-hydroxy-5-norbornene-2,3-dicarboximidenucleus, in order to identify selective ligands for the above-mentioned subtype receptors. Arylpiperazines represents one of the most important classes of 5-HT1AR ligands, and recent research concerning new derivatives has been focused on the modification of one or more portions of such pharmacophore. The combination of structural elements (heterocyclic nucleus, propyl chain and 4-substituted piperazine), known to be critical to the affinity to 5-HT1A receptors, and the proper selection of substituents led to compounds with high specificity and affinity towards serotoninergic receptors. The most active compounds were selected for further in vivo assays to determine their functional activity. Finally, to rationalize the obtained results, molecular docking studies were performed. The results of the pharmacological studies showed that Norbo-4 and Norbo-18 were the most active and promising derivatives for the serotonin receptor considered in this study. 相似文献