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81.
W. R. Schoeller A. R. Powell O. Hahn K. E. Pütter E. S. Simpson W. F. Hillebrand G. E. F. Lundell O. Ruff E. Schiller W. P. Headden H. Pied H. W. Webb R. J. Meyer O. Hauser W. B. Giles R. C. Wells E. F. Waterhouse G. T. Prior E. C. Deering L. Finckh J. H. Muller J. W. Mellor E. W. Todd V. Schwarz G. W. Sears W. D. Treadwell 《Analytical and bioanalytical chemistry》1934,99(5-6):205-227
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J. Bicskei A. Dubose E. Spitalsky S. Jofa D. Dobrosserdow F. Dienert W. S. Iofinow W. W. Scott G. G. Kandilarow D. S. Reynols W. H. Ross K. D. Jacob N. K. Smit L. D. Hammond A. Travers H. Ginsberg G. Holder B. Thèphile H. ter Meulen P. Drawe G. E. F. Lundell und J. I. Hoffmann 《Fresenius' Journal of Analytical Chemistry》1930,81(5-7):232-242
Ohne Zusammenfassung 相似文献
84.
N. Allen N. H. Furman E. Krause R. Becker P. Pfeiffer K. Schnurmann R. F. Chambers Ph. C. Scherer W. F. Hillebrand G. E. F. Lundell D. S. Reynolds W. H. Roß K. D. Jacob O. B. Winter Lillian Butler F. J. Frere G. Batchelder V. W. Meloche I. Tananaeff H. Flisik E. C. Roper E. B. R. Prideaux P. Drawe W. Rehwinkel L. Dupare P. Wenger G. Graz 《Analytical and bioanalytical chemistry》1934,96(5-6):211-223
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Dihydrothiazolo ring-fused 2-pyridones have previously been shown to inhibit pilus assembly in uropathogenic Escherichia coli. Methods have now been developed to synthesize both dihydroimidazolo and dihydrooxazolo ring-fused 2-pyridones. To obtain the nitrogen analogs, Cbz-protected imidazolines were reacted with an acyl-Meldrum's acid derivative under acidic conditions. To prepare the oxygen analogs, a one-pot procedure was developed that allowed synthesis of dihydrooxazolo ring-fused 2-pyridones starting from acylated serine derivatives. After hydrolysis to their corresponding carboxylic acids and lithium carboxylates, biological evaluation revealed that the sulfur could be replaced by an oxygen atom and still maintains the ability to inhibit pilus assembly in uropathogenic E. coli. However, introducing a secondary amine instead of oxygen resulted in a substantial decrease in biological activity. 相似文献
88.
A simple and rapid multicomponent screening method of 130 substances for direct injections of urine samples has been developed. The fully automated method based on ultra-performance liquid chromatography (UPLC) and tandem mass spectrometry (MS/MS) is used for three different classes of doping agents: diuretics, central nervous system stimulants (CNS stimulants) and opiates. The samples are diluted with buffer containing internal standards (IS) by a pipetting robot system into 96-well plates. Samples are injected on a reversed phase sub 2-microm particle column connected to a fast polarity switching and rapid scanning tandem mass spectrometer with an electrospray interface. The software used to evaluate the results produced reports containing a small-sized window for each component and a data table list with flags to indicate any adverse analytical findings in the sample. The report can also be processed automatically using an application software, which interpret the data and indicate if there is a suspicious sample. One 96-well plate can be analyzed within 16 h. 相似文献
89.
Tholander F Muroya A Roques BP Fournié-Zaluski MC Thunnissen MM Haeggström JZ 《Chemistry & biology》2008,15(9):920-929
M1 aminopeptidases comprise a large family of biologically important zinc enzymes. We show that peptide turnover by the M1 prototype, leukotriene A4 hydrolase/aminopeptidase, involves a shift in substrate position associated with exchange of zinc coordinating groups, while maintaining the overall coordination geometry. The transition state is stabilized by residues conserved among M1 members and in the final reaction step, Glu-296 of the canonical zinc binding HEXXH motif shuffles a proton from the hydrolytic water to the leaving group. Tripeptide substrates bind along the conserved GXMEN motif, precisely occupying the distance between Glu-271 and Arg-563, whereas the Arg specificity is governed by a narrow S1 pocket capped with Asp-375. Our data provide detailed insights to the active site chemistry of M1 aminopeptidases and will aid in the development of novel enzyme inhibitors. 相似文献
90.
Lignell A Lundell J Khriachtchev L Räsänen M 《The journal of physical chemistry. A》2008,112(24):5486-5494
The complexes of xenon hydrides HXeY (Y = Cl and Br) with hydrogen halides HX (X = Cl and Br) have been studied both computationally and experimentally in a xenon matrix. The experiments revealed three new complexes: HXeBr...HBr, HXeBr...HCl, and HXeCl...HCl. The experimental assignments were done on the basis of the strong H-Xe stretching absorption of HXeY (Y = Cl and Br) molecules and supported by theoretical results. We experimentally obtained monomer-to-complex blue-shifts of this vibrational mode for all the studied systems (up to approximately 150 cm (-1)). The electronic structure calculations revealed three local structures for each HNgY...HX complexes and their computed interaction energies varied between -460 and -2800 cm (-1). The computational estimates of the vibrational shifts were in agreement with the experimental values. We also found possible experimental absorption belonging to HXeBr...(HBr) 2 trimer and its vibrational shift (+245 cm (-1)) is similar to the computational estimate of a cyclic ternary complex (+252 cm (-1)). 相似文献