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101.
Sakamoto I Nishii T Ozaki F Kaku H Tanaka M Tsunoda T 《Chemical & pharmaceutical bulletin》2005,53(11):1508-1509
(Cyanomethylene)tributylphosphorane (CMBP), which promoted the alkylation of various nucleophiles (HA) with alcohols (ROH) to give RA (Mitsunobu-type reaction), was prepared in two steps starting from chloroacetonitrile. 相似文献
102.
Togawa Y Harada K Akashi T Kasai H Matsuda T Nori F Maeda A Tonomura A 《Physical review letters》2005,95(8):087002
Using Lorentz microscopy to directly image vortices, we investigate vortex motion control and rectification in a niobium superconductor. We directly observe a net motion of vortices along microfabricated channels with a spatially asymmetric potential, even though the vortices were driven by an oscillatory field. By observing the individual motion of vortices, we clarify elementary processes involved in this rectification. To further demonstrate the ability to control the motion of vortices, we created a tiny vortex "racetrack" to monitor the motion of vortices in a closed circuit channel. 相似文献
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Nobuhito Ito Hiroto Kudo Atsushi Kameyama Tadatomi Nishikubo Tetsuo Anada 《Journal of polymer science. Part A, Polymer chemistry》2003,41(1):213-222
The synthesis and optical properties of polyesters with pendant fluorinated phenoxy groups were examined. The polyaddition of bisphenol AF diglycidyl ether ( 1 ) with fluorine‐containing terephtalates ( 2a–f ) was carried out with tetrabutylphosphonium chloride (TBPC) as the catalyst in chlorobenzene to afford the corresponding polyesters with number‐average molecular weights (Mn's) ranging from 15,200 to 30,000 in 88–96% yields. Furthermore, the polyaddition of 1 with isophthalate 2g and phthalate 2h also produced high‐molecular‐weight polyesters with Mn's = 22,700 and 22,600 in 88 and 84% yields, respectively. The linear relationship was observed between the fluorine contents and refractive indices of the obtained polyesters. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 213–222, 2003 相似文献
105.
Time-resolved absorption spectra of the A exciton in CdSe are measured by using pico-second white-light pulses produced by a self-phase modulation technique. The absorption peak of the n = 1 A exciton shifts to the high-energy side due to the high-density effect. The magnitude of the shift reaches a maximum at 20 psec after the pulse excitation, which is considered to indicate that the time constant for the formation of the n = 1 excitons by band-to-band excitation is about 20 psec. 相似文献
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As part of a series of elucidation of the structural features of peptides caused by C-terminal alpha-amidation, the crystal structures of H-Val-Gly-NH2, H-Ser-Phe-NH2, H-Gly-Tyr-NH2, and H-Pro-Tyr-NH2 hydrochloride salts were analyzed by the X-ray diffraction method. Although respective molecules take energetically allowable torsion angles concerning the backbone and side chains, their conformations are not necessarily the same as the corresponding unamidated ones. This results from the different molecular packing requirements, rather than from different conformational features inherent in the C-amidated and -unamidated peptides. As for the molecular packing feature, each peptide tended to form a repeated structure through those hydrogen bonds in which both amide NH and O=C groups participate. The chloride ions are located between the neighboring peptides and are hydrogen-bonded to the respective amide NHs, leading to the sheet structure. The hydrogen-bonding feature of the amide group and its function in molecular packing was discussed based on the results analyzed so far. 相似文献
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Coupling Reaction of Enol Derivatives with Silyl Ketene Acetals Catalyzed by Gallium Trihalides
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Dr. Yoshihiro Nishimoto Yuji Kita Hiroki Ueda Hiroto Imaoka Kouji Chiba Prof. Dr. Makoto Yasuda Prof. Dr. Akio Baba 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(33):11837-11845
A cross‐coupling reaction between enol derivatives and silyl ketene acetals catalyzed by GaBr3 took place to give the corresponding α‐alkenyl esters. GaBr3 showed the most effective catalytic ability, whereas other metal salts such as BF3?OEt2, AlCl3, PdCl2, and lanthanide triflates were not effective. Various types of enol ethers and vinyl carboxylates as enol derivatives are amenable to this coupling. The scope of the reaction with silyl ketene acetals was also broad. We successfully observed an alkylgallium intermediate by using NMR spectroscopy, suggesting a mechanism involving anti‐carbogallation among GaBr3, an enol derivative, and a silyl ketene acetal, followed by syn‐β‐alkoxy elimination from the alkylgallium. Based on kinetic studies, the turnover‐limiting step of the reaction using a vinyl ether and a vinyl carboxylate involved syn‐β‐alkoxy elimination and anti‐carbogallation, respectively. Therefore, the leaving group had a significant effect on the progress of the reaction. Theoretical calculations analysis suggest that the moderate Lewis acidity of gallium would contribute to a flexible conformational change of the alkylgallium intermediate and to the cleavage of the carbon?oxygen bond in the β‐alkoxy elimination process, which is the turnover‐limiting step in the reaction between a vinyl ether and a silyl ketene acetal. 相似文献