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91.
Madlene U. Koller Katrina L. Peariso Tina S. Guion Shannon Studer Martinez Charles F. Beam 《合成通讯》2013,43(19):2963-2974
2-, 3-, or 4-Picolyllithium was prepared in excess lithium diiso-propylamide and condensed with several hydroxy-benzaldehydes and 4-hydroxy-acetophenone to afford substituted hydroxyphenyl-pyridyl-ethanols and α-hydroxyphenyl-α-methylpyridineethanols. In two instances. 3-picolyllithium condensed with aldehydes to presumably form the hydroxyphenyl-pyridyl-ethanol, which underwent linear dehydration to the substituted pyridyl-ethylenyl-phenol. 相似文献
92.
Oxidation of a β-aziridinyl alcohol with tetrapropylammonium perruthenate yields a pyrrole and two unusual imine derivatives of fumaraldehyde. 相似文献
93.
94.
95.
David S. Weinberg M. Lisa Manier Mark D. Richardson Frederick G. Haibach Tina S. Rogers 《Journal of separation science》1992,15(10):641-654
Nine organosulfur compounds present in an aged garlic extract and two isoflavonoids and one triterpenoid present in a licorice root extract powder have been identified and quantified. Quantification involved solvent extraction and gas chromatographic – mass spectrometric analysis (garlic extract) or hydrolysis, solvent extraction, and liquid chromatographic analysis (licorice root extract powder). Although the garlic extract proved to be unstable and the concentration of the organosulfur compounds varied with time, one analysis of the extract gave the following results: methyl disulfide (0.607 μg/g), methyl trisulfide (0.181 μg/g), allyl sulfide (2.02 μg/g), allyl disulfide (0.784 μg/g), allyl trisulfide (0.795 μg/g), allyl methyl sulfide (1.64 μg/g), allyl methyl disulfide (0.411 μg/g), allyl methyl trisulfide (0.695 μg/g), and ethyl 2-propenesulfinate (11.4 μg/g). The analysis of the licorice root extract powder gave the following results: formononetin (1.92 mg/g), isoliquiritigenin (9.61 mg/g), and 18β-glycyrrhetinic acid (43.9 mg/g). Methods were successfully developed to quantify the same compounds in the serum of test animals which had consumed feed spiked with garlic extract or licorice root extract powder. Only the 18β-glycyrrhetinic acid could be detected in the sera of such animals, however. An effort was also made to determine serum levels of prostaglandin E2 to correlate its inhibition with levels of the dietary components, but the prostaglandin E2 levels were too low to measure. 相似文献
96.
We describe explicitly each stage of a numerically stable algorithm for calculating with exponential tension B-splines with
non-uniform choice of tension parameters. These splines are piecewisely in the kernel of D
2(D
2–p
2), where D stands for ordinary derivative, defined on arbitrary meshes, with a different choice of the tension parameter p on each interval. The algorithm provides values of the associated B-splines and their generalized and ordinary derivatives
by performing positive linear combinations of positive quantities, described as lower-order exponential tension splines. We
show that nothing else but the knot insertion algorithm and good approximation of a few elementary functions is needed to
achieve machine accuracy. The underlying theory is that of splines based on Chebyshev canonical systems which are not smooth
enough to be ECC-systems. First, by de Boor algorithm we construct exponential tension spline of class C
1, and then we use quasi-Oslo type algorithms to evaluate classical non-uniform C
2 tension exponential splines.
相似文献
97.
98.
[reaction: see text] There is substantial isomerization (kiso=0.32 x 10(-3) s(-1)) of 3-NO2C6H4(13)CH(Me)OS(18O)2Tos during solvolysis (ksolv=1.04 x 10(-3) s(-1)) in 50/50 trifluoroethanol/water, even though the estimated lifetime of the putative 1-(3-nitrophenyl)ethyl carbocation intermediate of solvolysis (ca. 10(-13) s(-1)) is too short to allow rearrangement that exchanges the positions of 16O and 18O at the sulfonate leaving group. This suggests that isomerization proceeds by a mechanism that avoids formation of the carbocation-anion pair intermediate. 相似文献
99.
Determination of chloramphenicol in bovine milk by liquid chromatography/tandem mass spectrometry 总被引:2,自引:0,他引:2
A rapid confirmatory liquid chromatographic/tandem mass spectrometic method was developed for determination of chloramphenicol in bovine milk. Chloramphenicol was extracted directly from milk by solid-phase extraction on a C18 cartridge. The extract was further cleaned up on neutral aluminium oxide. Three transition products were monitored in negative ion mode after atmospheric pressure chemical ionization. The detection capability related to the transition product of lowest abundance was 0.03 microg/kg. The mean recovery was 90% at levels of 0.1-0.2 microg/kg. The relative repeatability standard deviations were 4.3, 3.8, and 2.8% at levels of 0.1, 0.2, and 1.0 microg/kg, respectively. 相似文献
100.
In this study, it is shown that calibration solution prepared in control matrix extrix extract can be used to compensate for matrix-induced chromatographic response enhancement observed for certain pesticedes. This phenomenon is characterized by enhanced chromatographic response for certain pesticides in the presence of matrix du to reduced analyte loss during injection. Unacceptably high recoveries are seen for affected pesticides when maatrix-free solutions are used for reference and calibration. The effects of matrix concentration on overall enhancement and linear response were determined. When used as reference standards for the determination of recovery, matrix-standard solutions were found to provide acceptable recoveries for pesticides subject to matrix-induced chromatographic response enhancement along with other pesticides. General guidelines are presented for using matrix-standard calibration solutions in pesticide residue analysis. 相似文献