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31.
The synthesis of a novel class of aminoglycoside, pyranmycin, and a convenient method for the preparation of 6-amino-L-idopyranosides were reported. One of the members in the reported pyranmycin families, TC010, has prominent activity against Escherichia coli, Staphylococcus aureus, and Bacillus megaterium. We also discovered that the (4)C(1) chair conformation on ring III of pyranmycin is essential for the antibacterial activity. [reaction: see text] 相似文献
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Shinji Fushiya Yoshikazu Sato Shigeo Nozoe Kyosuke Nomoto Tsunematsu Takemoto Sei-ichi Takagi 《Tetrahedron letters》1980,21(32):3071-3072
A new amino acid derivative possessing an iron chelating activity was isolated from root washings of water cultured under iron deficient conditions. The structure of this compound, avenic acid A has been determined as 2(S),3′(S),3″(S)-N-[3-(3-hydroxy-3-carboxypropylamino)-3-carboxypropyl]-homoserine (1) on the basis of chemical and spectroscopic evidence. 相似文献
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Troxel D. Schreiber W. Bishop R. Buckley R. Bunza G. Eguchi T. Goldwasser S. Jakubson J. Jung-Shu Kung Ng D. Takemoto S. Yokoyama E. 《Communications, IEEE Transactions on》1981,29(12):1841-1848
The two-channel system previously reported has been implemented in hardware using system parameters appropriate to consumer television. The basic system divides the spectrum into lowand high-frequency spatial components. The lows are coarsely sampled and finely quantized and the highs finely sampled and coarsely quantized using a companded, randomized quantizer. The purpose of this experiment was to demonstrate the potential of the system for low-cost practical application, to study the effect of the character of the randomizing noise, and to ascertain that there were no deleterious effects due to interlace, motion, or input noise. Theoretical noise calculations were qualitatively confirmed. 相似文献
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Takemoto Y 《Organic & biomolecular chemistry》2005,3(24):4299-4306
Hydrogen-bonding interaction plays a crucial role in the molecular recognition and activation processes of various biologically important reactions that are mediated by enzymes and antibodies in living organisms. Recently, it has been shown that a hydrogen-bonding donor can be used as a general acid catalyst for various types of reactions in organic chemistry. In this article, we describe enantioselective reactions catalyzed by urea and thiourea derivatives as general acid catalysts as well as diastereoselective reactions. This perspective provides an overview of this rapidly growing field. 相似文献
38.
Allylation and propargylation of glyoxylic oxime ether in the presence of a catalytic amount of palladium(0) complex and indium(I) iodide were studied. Excellent diastereoselectivities in allylation were achieved in the presence of water, although low diastereoselectivities were observed in the absence of water. Propargylation of glyoxylic oxime ether proceeded with good diastereoselectivities in the presence of LiBr or LiCl. 相似文献
39.
Takeishi S Rant U Fujiwara T Buchholz K Usuki T Arinaga K Takemoto K Yamaguchi Y Tornow M Fujita S Abstreiter G Yokoyama N 《The Journal of chemical physics》2004,120(12):5501-5504
DNA oligo-nucleotides, localized at Au metal electrodes in aqueous solution, are found to be released when applying a negative bias voltage to the electrode. The release was confirmed by monitoring the intensity of the fluorescence of cyanine dyes (Cy3) linked to the 5' end of the DNA. The threshold voltage of the release changes depending on the kind of linker added to the DNA 3'-terminal. The amount of released DNA depends on the duration of the voltage pulse. Using this technique, we can retain DNA at Au electrodes or Au needles, and release the desired amount of DNA at a precise location in a target. The results suggest that DNA injection into living cells is possible with this method. 相似文献
40.
Takemoto S Kobayashi T Matsuzaka H 《Journal of the American Chemical Society》2004,126(35):10802-10803
Treatment of a dinuclear Ru(II) amido complex [Cp*Ru(mu2-NHPh)]2 (Cp* = eta5-C5Me5) with small organic substrates including CO, tert-butyl isocyanide, a sulfur ylide Ph2S=CH2, and diphenylacetylene resulted in an unexpected disproportionation reaction of the bridging amido ligands to produce a free amine and a series of imido-bridged diruthenium complexes [(Cp*Ru)2(mu2-L)(mu2-NPh)] (L = CO, t-BuNC, CH2). In the case of diphenylacetylene, the bridging imido ligand underwent subsequent coupling reaction with the coordinated alkyne to form an iminoalkenyl complex [(Cp*Ru)2(mu2-PhNCPhCPh)]. 相似文献