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81.
Cavaliere C Foglia P Pastorini E Samperi R Laganà A 《Rapid communications in mass spectrometry : RCM》2005,19(21):3143-3158
A mass spectrometric method for extensive detection and semi-quantitative determination of flavonoid glycosides in stem and leaves of young Triticum durum plants is presented. About 100 g of sample were lyophilized and ground, and the compounds of interest were then extracted, cleaned-up, and fractionated using high-performance liquid chromatography (HPLC). Tandem mass spectrometry analyses were performed using a quadrupole-linear ion trap instrument with an information-dependent data acquisition (IDA) protocol that looped two experiments, enhanced MS scan and enhanced product ion scan. Various glycoconjugates, which are all derivatives of only four flavones, apigenin, luteolin, chrysoeriol and tricin, were identified and belong to the following categories: 7 monoglycosides, 31 diglycosides, 15 triglycosides and 1 tetraglycoside. Among these some acylated glycosides were found. Tricin derivatives are present exclusively as O-glycosides, while apigenin and luteolin are present always as C-glycosides. Semi-quantitative estimation was performed by using the monoglycoside and diglycoside of quercetin as internal standards. 相似文献
82.
Patrizia Ciminiello Carmela Dell'Aversano Martino Forino Federico Umberto Santelia Emmanuel N. Pitsinos 《Tetrahedron》2006,62(33):7738-7743
The analysis of a batch of toxic mussels (Mytilus galloprovincialis) from the Northern Adriatic Sea led to the isolation of a novel oxazinin, oxazinin-4. Its structure including the relative stereochemistry has been elucidated through extensive NMR analysis. A synthetic route to oxazinins has been crucial in establishing the absolute stereochemistry of oxazinin-4 and for reassigning the absolute C-2 configuration of oxazinin-1 and -2 previously isolated from toxic shellfish and stereostructurally characterized. 相似文献
83.
84.
Natural estrogens in dairy products: Determination of free and conjugated forms by ultra high performance liquid chromatography with tandem mass spectrometry 下载免费PDF全文
Chiara Cavaliere Anna Laura Capriotti Patrizia Foglia Susy Piovesana Roberto Samperi Salvatore Ventura Aldo Lagan 《Journal of separation science》2015,38(20):3599-3606
Natural estrogens are synthesized by mammals in different amounts depending on the developmental stage and pregnancy/lactation period, and they may pass into milk, where they are mostly present as glucuronated and sulfated forms. In modern dairy practices, about 75% of milk is produced from pregnant cows; therefore, the amount of hormones that may pass into milk could be of concern. While estrogen determination in milk has been investigated in depth, the individual determination of estrogens and their conjugated forms in dairy products has not been fully addressed. The aim of this work was to develop and assess a sensitive method, using the peculiar retention properties of graphitized carbon black, to extract natural free estrogens and their major conjugated metabolites, without any enzymatic cleavage, from yogurt, cheese, and butter. The free and conjugated estrogens were eluted in two distinct fractions from the solid‐phase extraction cartridge and analyzed separately by ultra high performance liquid chromatography coupled to tandem mass spectrometry. Recoveries were higher than 80% for all the three sample typologies. The highest matrix effects were observed for butter, which was richest in lipid content, but was below 30%. A survey on some commercial dairy products suggests that production processes decreased estrogen content. 相似文献
85.
The CD curves of a set of condensed γ-butyrolactones have been investigated. A simple correlation between the sign of the Cotton effect (CE) and the configuration of C can be deduced from the resulting data. 相似文献
86.
87.
Patrizia Ferraboschi Maria De Mieri Fiorella Galimberti 《Tetrahedron: Asymmetry》2010,21(17):2136-2141
The (S)-2-chlorophenylglycine moiety is well recognized in the structure of (S)-clopidogrel, a known antithrombotic drug. We prepared an enantiomerically pure chiral building block via an enzyme-catalyzed resolution of (RS)-N-Boc-2-chlorophenylglycine methylester. The best results were obtained by means of an immobilized subtilisin, the cross-linked enzyme aggregate (Alcalase-CLEA®). The high enantiomeric excess of the synthon obtained remained the same over the course of clopidogrel synthesis; the simplicity of the process makes this pathway suitable for large-scale preparation. 相似文献
88.
A classical system for the preparation of carbonyl compounds from alkenes relies upon ozonolysis of the double bond, followed by reductive cleavage of the ozonide so formed. Among the reagents of choice for such a reduction, triphenylphosphine certainly has enjoyed a widespread use.1 However, in spite of the simplicity of the method, often one can face problems in the purification of the carbonyl compound from unreacted triphenylphosphine, especially if the polarities of both products are very similar. We have encountered such a problem during the preparation of the (20 S)-6β -ethoxy-3 α, 5-cyclo-5α -pregnane-20-carbaldehyde 4 from the suitably protected stigmasterol32. In this case, when triphenylphosphine was used for reduction of ozonide we never could isolate the aldehyde 2 uncontaninated by tripherylphosphine. 相似文献
89.
Margherita Bernardeschi Patrizia Guidi Vittoria Scarcelli Giada Frenzilli Marco Nigro 《Analytical and bioanalytical chemistry》2010,396(2):619-623
Titanium dioxide is extensively used in a variety of products, including industrial materials and cosmetics. Studies mainly
performed on human cell lines and in vivo exposure on experimental animals have raised concern about the toxic effects of
ultrafine titanium dioxide; however, scarce information is available about its impact on aquatic life. The aim of this article
was to assess the genotoxic potential of TiO2 (anatase and rutile) on bottlenose dolphin leukocytes. Blood samples were obtained from four male and one female specimens
reared at the Adriatic SeaWorld “Oltremare” (Riccione, Italy). Leukocytes were isolated by the lyses procedure and in vitro
exposed to TiO2 in RPMI. Experimental solutions were sonicated immediately before dosing the cells. Three exposure times (4, 24 and 48 h)
and three doses (20, 50 and 100 μg/ml) were tested. Genotoxicity was detected by the single-cell gel electrophoresis (or comet
assay) at pH ≥ 13, assessing single/double-strand breaks and alkali-labile sites. Cytotoxicity was also detected by the Trypan
blue exclusion method. Results showed that both the crystalline forms of TiO2 were genotoxic for bottlenose dolphin leukocytes, with a statistically significant increase of DNA fragmentation after exposure
to 50 and 100 μg/ml for 24 and 48 h. Although preliminary, these are the first data regarding the genetic susceptibility of
toothed cetaceans toward an “emerging” pollutant, such as TiO2 particles. 相似文献
90.
Patrizia Di Gennaro Silvana Bernasconi Fulvia Orsini Erika Corretto Guido Sello 《Tetrahedron: Asymmetry》2010,21(15):1885-1889
The use of two oxidoreductases (an aldoketo reductase from Escherichia coli JM109 and an alcohol dehydrogenase from Lactobacillus brevis) has demonstrated that it is possible to prepare enatiomerically pure diols in a one-pot operation. The reactions were applied to the synthesis of (1R)-1-[3-(hydroxymethyl)phenyl]ethanol and (1S)-1-phenylethane-1,2-diol, using a two-step procedure. The yield is nearly quantitative and the enantiomeric purity is greater than 95%. A third step has been introduced by adding a cell biocatalyst showing dihydrodiol dehydrogenase activity from Pseudomonas fluorescens N3. This allows for the preparation of 3-[(1R)-1-hydroxyethyl]benzoic acid and (2S)-hydroxy(phenyl)ethanoic acid. 相似文献