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991.
992.
Dr. Filippo Sladojevich Ángel L. Fuentes de Arriba Dr. Irene Ortín Dr. Ting Yang Dr. Alessandro Ferrali Dr. Robert S. Paton Prof. Darren J. Dixon 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(42):14286-14295
The enantioselective Conia‐ene cyclization of alkyne‐tethered β‐ketoesters is efficiently catalyzed by the combination of cinchona‐derived amino‐urea pre‐catalysts and copper(I) salts. The reaction scope is broad and a series of substrates can be efficiently cyclized with high yields and enantioselectivities. Herein, we present a detailed mechanistic study based on experimental considerations and quantum mechanical calculations. Several variables, such as the nature of the organic pre‐catalyst and the metal‐ion source, have been thoroughly investigated. Kinetic studies, as well as kinetic isotope effects and deuterium labeling experiments have been used to gain further insights into the mechanism and prove the cooperative nature of the catalytic system. Our studies suggest that the rate‐limiting step for the reaction involves the β‐ketoester deprotonation and that the active species responsible for the enantiodeterming step is monomeric in amino‐urea pre‐catalyst. Computational studies provide a quantitative understanding of the observed stereoinduction and identify hydrogen bonding from the urea group as a crucial factor in determining the observed enantioselectivity. 相似文献
993.
Andr Augusto Gomes Faraco Jos Dias De Souza Filho Maria Auxiliadra Fontes Prado Ricardo Jos Alves Renata Fontes Prado Norma Beatriz D'Accorso 《Journal of heterocyclic chemistry》1999,36(5):1129-1133
The tetrazoles 5-(6′-acetamido-6′-deoxy-1′,2′:3′,4′-di-O-isopropylidene-D-glycero-α-D-galactohexopyranos-6′-yl)tetrazole ( 1 ) and 5-(6′-acetamido-6′-deoxy-1′,2′:3′,4′–di-O-isopropylidene-L-glycero-α-D-galacto-hexopyranos-6′-yl)-tetrazole ( 2 ) were synthesized by the 1,3-dipolar cycloaddition reaction of the epimeric α-acetamidonitriles 5 and 6 , respectively, with sodium azide. Reaction of tetrazole 1 with acetic anhydride in the presence of pyridine afforded the N-acetyl-1,3,4-oxadiazole derivative 3 and the N-acetylacetamido-1,3,4-oxadiazole derivative 7 . The N-acetylacetamido-1,3,4-oxadiazole derivative ( 8 ) was isolated when the tetrazole 2 was allowed to react under the same conditions. The physical and spectroscopic data of the five new compounds 1, 2, 3, 7 and 8 are presented. 相似文献
994.
Fernández-Argüelles MT Cañabate B Segura A Costa JM Pereiro R Sanz-Medel A Fernández A 《Talanta》2005,66(3):696-702
A sensitive and selective phosphorimetric method for the determination of 1-naphthaleneacetic acid (1-NAA) based on a flow-injection system connected to a flow cell packed with a solid support and placed in the sample compartment of a conventional luminescence spectrometer is described. A non-ionic solid polymeric resin Amberlite XAD-7 is used for the packing. After injection of the sample, 1-NAA is on-line retained in the packed resin and measurements of the heavy atom induced (HAI)-room temperature phosphorescence (RTP) emission (λex/λem = 292/490 nm) from this native luminescent compound are taken.The optimum experimental conditions were investigated by injecting 2 ml samples of an aqueous solution of 1-NAA in the flow system. A concentration 0.15 mol l−1 of thallium(I) ions, as heavy atom, both in the samples and the carrier flow, was finally selected. Also, a concentration of 6 mmol l−1 of sulphite was optimal for ensuring the necessary deoxygenation of the system at the selected flow rate of 0.8 ml min−1. After measurement, the solid support was efficiently regenerated by injecting 1 ml of a mixture water:acetone in a ratio 1:1 (v/v) into the flow.The detection limit (3σ criterion) was 1.2 ng ml−1 of 1-NAA. The repeatability (R.S.D.) for five replicates of a sample containing 50 ng ml−1 of analyte turned out to be ±3% and the calibration graphs proved to be linear up to 500 ng ml−1 of 1-NAA (maximum concentration assayed). The effect of potential interferences from other organic species which can be also used as plant growth regulators, as well as from various inorganic cations and anions, has been investigated as well.The method was successfully applied to the determination of low levels of this plant growth regulator in natural waters (river and fountain waters) and apples. 相似文献
995.
Titanium complexes bearing an unprecedented tridentate cyclopentadienyl-silsesquioxanate ligand provide a new class of efficient and selective catalysts for epoxidation of olefins with aqueous hydrogen peroxide under homogeneous conditions. 相似文献
996.
Rios BE Sood P Klichko Y Koutha M Powell D Lattman M 《Dalton transactions (Cambridge, England : 2003)》2012,41(22):6677-6682
Treatment of a bis(phenylphosphonite)calix[5]arene ligand with either palladium(II) chloride or 1,5-cyclooctadieneplatinum(II) chloride yields square planar metal complexes in which the two phosphorus atoms bind cis to the MCl(2) moiety (M = Pd, Pt). Chloride was removed from the palladium complex to open a coordination site at the metal for catalysis. The chloride removal resulted in a rare and unexpected η(6) coordination of an arene to the metal. The reaction is reversible upon addition of tetra-n-butyl ammonium chloride. 相似文献
997.
S Sorribas B Zornoza C Téllez J Coronas 《Chemical communications (Cambridge, England)》2012,48(75):9388-9390
Silica-(ZIF-8) core-shell spheres with tuneable ordered meso-microporosity have been synthesized, showing that the hydrophobic micropore ZIF-8 shell controls the access of guest molecules into the hydrophilic silica mesoporous structure. 相似文献
998.
Elena Maria Yubero-Serrano Javier Delgado-Lista Patricia Pe?a-Orihuela Pablo Perez-Martinez Francisco Fuentes Carmen Marin Isaac Tunez Francisco Jose Tinahones Francisco Perez-Jimenez Helen M Roche Jose Lopez-Miranda 《Experimental & molecular medicine》2013,45(6):e28
Previous evidence supports the important role that oxidative stress (OxS) plays in metabolic syndrome (MetS)-related manifestations. We determined the relationship between the number of MetS components and the degree of OxS in MetS patients. In this comparative cross-sectional study from the LIPGENE cohort, a total of 91 MetS patients (43 men and 48 women; aged between 45 and 68 years) were divided into four groups based on the number of MetS components: subjects with 2, 3, 4 and 5 MetS components (n=20, 31, 28 and 12, respectively). We measured ischemic reactive hyperemia (IRH), plasma levels of soluble vascular cell adhesion molecule-1 (sVCAM-1), total nitrite, lipid peroxidation products (LPO), hydrogen peroxide (H2O2), superoxide dismutase (SOD) and glutathione peroxidase (GPx) plasma activities. sVCAM-1, H2O2 and LPO levels were lower in subjects with 2 or 3 MetS components than subjects with 4 or 5 MetS components. IRH and total nitrite levels were higher in subjects with 2 or 3 MetS components than subjects with 4 or 5 MetS components. SOD and GPx activities were lower in subjects with 2 MetS components than subjects with 4 or 5 MetS components. Waist circumference, weight, age, homeostatic model assessment-β, triglycerides (TGs), high-density lipoprotein and sVCAM-1 levels were significantly correlated with SOD activity. MetS subjects with more MetS components may have a higher OxS level. Furthermore, association between SOD activity and MetS components may indicate that this variable could be the most relevant OxS biomarker in patients suffering from MetS and could be used as a predictive tool to determine the degree of the underlying OxS in MetS. 相似文献
999.
José Villamizar Federico Plata Nieves Canudas Eleonora Tropper Juan Fuentes Angel Orcajo 《合成通讯》2013,43(3):311-320
A facile access to optically active (+)‐ent‐chromazonarol ent‐1, isolated from the sponge Disidea pallescens, is reported from commercially available (+)‐manool 4. 相似文献
1000.
M. Antnia Nunes Filip Reszczyski Ricardo N. M. J. Pscoa Anabela S. G. Costa Rita C. Alves Maria Beatriz P. P. Oliveira 《Molecules (Basel, Switzerland)》2021,26(1)
Food innovation is moving rapidly and comprises new categories of food products and/or ingredients with a natural and ecological origin. Monocultivar olive pomaces, individually or combined, can be a source of natural bioactive compounds suitable for food or cosmetic applications. This work aimed to assess the phenolics content and antioxidant activity of four monocultivar olive pomaces (Arbosana, Koroneiki, Oliana, and Arbequina) and forty-nine blends prepared with different proportions of each. Additive, synergistic, and antagonistic effects were studied. Among the monocultivar pomaces, Koroneiki and Arbosana were the richest in total phenolics (~15 mg gallic acid eq./g). Most of the interactions found in the blends were additive or synergistic, while very few antagonistic effects were observed. The best results were obtained for those blends where the Koroneiki variety predominated: (i) 90% Koroneiki, 4.75% Oliana, 3.75% Arbequina, 1.5% Arbosana; (ii) 65% Koroneiki, 29% Oliana, 3.25% Arbequina, 2.75% Arbosana; and (iii) 85% Koroneiki, 8.75% Arbequina, 3.5% Arbosana, 2.75% Oliana. In sum, these combinations can be advantageous in comparison to the individual use of monocultivar pomaces, presenting a higher potential to be used as functional ingredients or for bioactive compounds extraction, having in view the obtention of natural preservatives or food/cosmetic formula enhancers. 相似文献