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81.
Dussault PH Lee IQ Lee HJ Lee RJ Niu QJ Schultz JA Zope UR 《The Journal of organic chemistry》2000,65(25):8407-8414
The Lewis acid-mediated reaction of alkene nucleophiles with peroxyacetals provides an effective route for the synthesis of homologated peroxides and hydroperoxides. In the presence of Lewis acids such as TiCl(4), SnCl(4), and trimethylsilyl triflate, peroxyacetals and peroxyketals undergo reaction with allyltrimethylsilane, silyl enol ethers, and silyl ketene acetals to afford homoallyl peroxides, 3-peroxyketones, and 3-peroxyalkanoates, respectively. Reactions of peroxyacetals are Lewis acid dependent; TiCl(4) promotes formation of ethers while SnCl(4) and trimethylsilyl triflate promote formation of peroxides. Lewis acid-promoted reactions of silylated hydroperoxyacetals furnish silylated hydroperoxides, which can be deprotected to homologated hydroperoxides. Hydroperoxyketals undergo Lewis acid-mediated allylation to furnish 1,2-dioxolanes via attack of hydroperoxide on the intermediate carbocation. Lewis acid-mediated cyclization of unsaturated peroxyacetals furnishes 1,2-dioxanes, 1,2-dioxepanes, and 1,2-dioxacanes through 6-endo/exo, 7-endo/endo, and 8-endo/endo pathways. The corresponding reactions involving 6-endo/endo and 5-endo/exo pathways were unsuccessful. 相似文献
82.
Belvisi L Bernardi A Checchia A Manzoni L Potenza D Scolastico C Castorina M Cupelli A Giannini G Carminati P Pisano C 《Organic letters》2001,3(7):1001-1004
[structure: see text]. A small library of cyclic RGD pseudopentapeptides incorporating stereoisomeric 6,5- and 7,5-fused bicyclic lactams was synthesized with the aim of developing active and selective integrin antagonists. The solid-phase synthesis and activity of these RGD derivatives is described. The approach led to two of the most active known inhibitors of alpha(V)beta3 receptor. 相似文献
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B. Bilwes R. Bilwes V. DAmico J.L. Ferrero G. Giardina R. Potenza 《Nuclear Physics A》1983,408(1):173-191
The one-proton and one-neutron transfer reactions in the interaction of 34S with incident 32S were studied in the 0–3.5 MeV excitation energy range of the exit nuclei. The experimental set-up (kinematic identification technique, implanted targets, etc.) has allowed an angular resolution of 0.2°, a mass resolution of 1.5% and a Q-value resolution of 0.35 MeV.Comparison with DWBA computations using an analytical approximation for the radial integral, with insertion of suitable recoil corrections, demonstrates the absorptive direct mechanisms of the reactions, even when double excitation of residual nuclei is present. The extracted values for the products of spectroscopic factors are in very good agreement with the known values and they are confirmed by EFR-DWBA computations. The selectivities of the reaction receive about the same contributions from the nuclear structure as from the specific reaction mechanism. 相似文献
87.
Stefania Ordanini Giuliano Zanchetta Vanessa Porkolab Christine Ebel Franck Fieschi Ileana Guzzetti Donatella Potenza Alessandro Palmioli Črtomir Podlipnik Daniela Meroni Anna Bernardi 《Macromolecular bioscience》2016,16(6):896-905
Glycodendrimers based on aromatic cores have an amphiphilic character and have been reported to generate supramolecuar assemblies in water. A new group of glycodendrimers with an aromatic rod‐like core were recently described as potent antagonists of DC‐SIGN‐mediated viral infections. A full characterization of the aggregation properties of these materials is presented here. The results show that these compounds exist mostly as monomers in water solution, in dynamic equilibrium with small aggregates (dimers or trimers). Larger aggregates observed by dynamic light scattering and transmission Electron Microscopy for some of the dendrimers are found to be portions of materials not fully solubilized and can be removed either by optimizing the dissolution protocol or by centrifugation of the samples.
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