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51.
Len F. Lee Francis M. Schleppnik Ronald W. Schneider Dwane H. Campbell 《Journal of heterocyclic chemistry》1990,27(2):243-245
Reaction of ethyl 4,4,4-trifluoroacetoacetate with methylhydrazine produced not only the previously reported 5-hydroxy-3-(trifluoromethyl)pyrazole 1 but also its unknown isomer the 3-hydroxy-5-(trifluoromethyl)pyrazole 4 . The structure assignments are established based on 13C nmr spectra. Compound 1 was converted to 5-chloro-3-(trifluoromethyl)pyrazolecarboxylic acid 3 in two steps. 相似文献
52.
The metabolism of (+/-)fenfluramine, 1-(m-trifluoromethylphenyl)-2-N-ethylpropane, an anoretic agent, was investigated in humans. The analysis method was based on the use of ion-exchange resin extraction, solid-phase purification on the Bond Elut1M C8 cartridge, gradient elution high-performance liquid chromatography, enzymic hydrolysis of conjugates, further purification by Bond Elut C8 cartridge, derivatisation and capillary column gas chromatography-mass spectrometry (GC-MS). After administration of a 1 mg kg-1 oral dose, four metabolites plus unchanged fenfluramine were recovered in the 0-24 h urine from human volunteers and characterised by GC-MS. In the conjugated form, fenfluramine, norfenfluramine and m-trifluoromethylhippuric acid were detected by GC-MS. In the aglycone form, the major metabolite, 1-(m-trifluoromethylphenyl)-1,2-propane diol (fenfluramine diol), was monitored using GC-MS. The mass spectral characteristics of the m-trifluoromethylhippuric acid methyl ester, 1-(m-trifluoromethylphenyl)-1,2-propane ditrifluoracetate derivatives and the norfenfluramine and fenfluramine free base obtained under electron-impact ionization are presented. The metabolism of fenfluramine is discussed including a metabolic pathway in man accounting for the formation of its biotransformation products. 相似文献
53.
L. Gillo S. E. Golbreich T. Nagoshi I. Nakagawa C. S. Piper W. C. Campbell Marion I. Hanna L. Palfray C. Rocchi R. del Monte R. Lechner M. Roß L. A. Ynalvez H. Lecoq Th. A. G. Haanappel Thérèse Jullig J. Barbière A. Lecco L. Lilic und P. M. Heertjes 《Fresenius' Journal of Analytical Chemistry》1943,125(3-4):133-137
Ohne Zusammenfassung 相似文献
54.
Ena L. Brown N. Campbell P. P. T. Sah T. Sh. Ma C. S. Marvel C. G. Gauerke E. L. Hill C. M. Suter W. Moffett T. Otterbacher F. C. Whitmore G. Barger F. Tutin W. O. Pool H. J. Harwood A. W. Ralston und H. S. Fry 《Fresenius' Journal of Analytical Chemistry》1943,125(1-2):62-63
Ohne Zusammenfassung 相似文献
55.
L. Gillo S. E. Golbreich T. Nagoshi I. Nakagawa C. S. Piper W. C. Campbell Marion I. Hanna L. Palfray C. Rocchi R. del Monte R. Lechner M. Roß L. A. Ynalvez H. Lecoq Th. A. G. Haanappel Thérèse Jullig J. Barbière A. Lecco L. Lilic P. M. Heertjes 《Analytical and bioanalytical chemistry》1943,125(3-4):133-137
56.
W. G. Campbell J. C. Mc Gowan St. A. Bryant A. J. Bailey A. Orup R. I. Thieme H. Bergström K. G. Trobeck P. W. Moryganow J. I. Wlassjuk N. K. Koshewnikowa G. S. Ssurta G. Jayme H. Pfretzschner R. Steinmann M. G. van Beckum G. J. Ritter J. H. Barbour C. F. Cross und E. J. Bevan 《Fresenius' Journal of Analytical Chemistry》1940,119(1-2):67-71
Ohne Zusammenfassung 相似文献
57.
W. G. Campbell L. H. Smith St. A. Bryant und A. Breazzano 《Fresenius' Journal of Analytical Chemistry》1939,118(1-2):63-65
Ohne Zusammenfassung 相似文献
58.
59.
Total synthesis of lucilactaene, a cell cycle inhibitor active in p53-inactive cells 总被引:2,自引:0,他引:2
Coleman RS Walczak MC Campbell EL 《Journal of the American Chemical Society》2005,127(46):16038-16039
Hetero-bis-metalated 1,3-butadiene is employed in the lynchpin coupling of synthetic fragments of the side chain of the antitumor agent, lucilactaene. Sequential Stille and Suzuki-Miyaura couplings interpolate this unique boron/tin diene into the pentaene chain. The total synthesis of lucilactaene was accomplished efficiently, in just eight linear steps. 相似文献
60.
A flow microcalorimeter/densimeter system has been commissioned to measure heat capacities and densities of solutions containing radioactive species as a function of temperature. Measurements were made for NaTcO4(aq) at six temperatures (189.15 K to 373.15 K for the heat capacities, 287.43 K to 396.67 K for the densities) over the molality range 0.01 to 0.29 mol-kg–1. Measurements for NaReO4(aq) (NaReO4 is a common nonradioactive analogue for NaTcO4) were made under similar conditions, but for eight temperatures and a more extensive range of molalities, 0.05 to 0.65 mol-kg–1. Heat capacities of NaCl(aq) reference solutions were also measured from 293.15 K to 398.15 K.The heat capacity and density data are analysed using Pitzer's ioninteraction model. Equations for the apparent molar heat capacities and volumes are reported. Values of the NaReO4(aq) partial molar heat capacities are compared to literature values based on integral heats of solution. The agreement between the two sets of NaReO4 results is good below 330 K, but only fair at the higher temperatures. Values of the partial molar volumes have also been derived. Using literature values and the results of our experiments, it is calculated that the disproportionation of hydrated TcO2(s) to form TcO
4
–
(aq) and Tc(cr) occurs more readily at high temperatures. The uncertainties introduced by using thermodynamic values for ReO
4
–
(aq), in the absence of values for TcO
4
–
(aq), are discussed. 相似文献