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951.
《合成通讯》2013,43(4):679-686
Abstract 2-(Cyclohex-2′-enyl)-5,5-dimethyl-3-hydroxycyclohex-2-enone undergoes regioselective heterocyclization to give bridged heterocycles 5a,b and 7 on treatment with pyridine hydrotribromide or hexamethylenetetramine hydrotribromide (1 h); or elemental bromine (7 h); N-iodosuccinimide in acetonitrile at 0–5°C (1 h) and conc. H2SO4 at 0–5°C (2 h), respectively. 相似文献
952.
《合成通讯》2013,43(18):3233-3241
Abstract A concise synthesis of (2E,4Z)-2,4-heptadien-1-ol and (2E,4Z)-2,4-heptadienal is presented. Commercially available (Z)-2-penten-1-ol was converted to ethyl-(2E,4Z)-2,4-heptadienoate by reaction with activated MnO2 and (carboethoxymethylene)triphenylphosphorane in the presence of benzoic acid as a catalyst. Ethyl-(2E,4Z)-2,4-heptadienoate was converted to (2E,4Z)-2,4-heptadien-1-ol with LiAlH4. The alcohol was partially oxidized to (2E,4Z)-2,4-heptadienal with MnO2. The title compounds are male-specific, antennally active volatile compounds from the Saltcedar leaf beetle, Diorhabda elongata Brulle (Coleoptera: Chrysomelidae) and have potential use in the biological control of the invasive weed saltcedar (Tamarix spp). 相似文献
953.
Yu‐Yang Xie Zhi‐Min Chen Hui‐Yun Luo Hui Shao Yong‐Qiang Tu Xiaoguang Bao Ren‐Fei Cao Shu‐Yu Zhang Jin‐Miao Tian 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(36):12621-12626
An enantioselective sulfenylation/semipinacol rearrangement of 1,1‐disubstituted and trisubstituted allylic alcohols was accomplished with a chiral Lewis base and a chiral Brønsted acid as cocatalysts, generating various β‐arylthio ketones bearing an all‐carbon quaternary center in moderate to excellent yields and excellent enantioselectivities. These chiral arylthio ketone products are common intermediates with many applications, for example, in the design of new chiral catalysts/ligands and the total synthesis of natural products. Computational studies (DFT calculations) were carried out to explain the enantioselectivity and the role of the chiral Brønsted acid. Additionally, the synthetic utility of this method was exemplified by an enantioselective total synthesis of (?)‐herbertene and a one‐pot synthesis of a chiral sulfoxide and sulfone. 相似文献
954.
Roly J. Armstrong Wasim M. Akhtar Tom A. Young Fernanda Duarte Timothy J. Donohoe 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(36):12688-12692
Hydrogen borrowing catalysis serves as a powerful alternative to enolate alkylation, enabling the direct coupling of ketones with unactivated alcohols. However, to date, methods that enable control over the absolute stereochemical outcome of such a process have remained elusive. Here we report a catalytic asymmetric method for the synthesis of enantioenriched cyclohexanes from 1,5‐diols via hydrogen borrowing catalysis. This reaction is mediated by the addition of a chiral iridium(I) complex, which is able to impart high levels of enantioselectivity upon the process. A series of enantioenriched cyclohexanes have been prepared and the mode of enantioinduction has been probed by a combination of experimental and DFT studies. 相似文献
955.
Junpeng Xie Xiaodan Li Haojie Lai Zhijuan Zhao Jinliang Li Wanggang Zhang Weiguang Xie Yiming Liu Wenjie Mai 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(41):14882-14889
Metal–organic framework‐derived NiCo2.5S4 microrods wrapped in reduced graphene oxide (NCS@RGO) were synthesized for potassium‐ion storage. Upon coordination with organic potassium salts, NCS@RGO exhibits an ultrahigh initial reversible specific capacity (602 mAh g?1 at 50 mA g?1) and ultralong cycle life (a reversible specific capacity of 495 mAh g?1 at 200 mA g?1 after 1 900 cycles over 314 days). Furthermore, the battery demonstrates a high initial Coulombic efficiency of 78 %, outperforming most sulfides reported previously. Advanced ex situ characterization techniques, including atomic force microscopy, were used for evaluation and the results indicate that the organic potassium salt‐containing electrolyte helps to form thin and robust solid electrolyte interphase layers, which reduce the formation of byproducts during the potassiation–depotassiation process and enhance the mechanical stability of electrodes. The excellent conductivity of the RGO in the composites, and the robust interface between the electrodes and electrolytes, imbue the electrode with useful properties; including, ultrafast potassium‐ion storage with a reversible specific capacity of 402 mAh g?1 even at 2 A g?1. 相似文献
956.
Raiane Aparecida LopesNeves Fausto MoreiraAraujo Felipe SiqueiraPacheco Gustavo ChevitareseAzevedo Maria Auxiliadora CostaMatos Renato CamargoMatos 《Electroanalysis》2019,31(3):496-503
Sunscreen agents and in particular UV filters are compounds added in different cosmetic formulations, that has the function of preventing damage caused by sun exposition. Therefore, this paper proposes the development of a simple, fast and reliable electroanalytical method utilizing square wave voltammetry (SWV) to the determination of Benzophenone‐3 (BZ‐3), camphor 4‐methylbenzylidene (MBC) and 2‐ethylhexyl‐4‐methoxycinnamate (OMC) in cosmetic samples. The electrochemical system consisted of a cell with three electrodes: work – gold electrode modified, reference – Ag/AgCl(sat) and auxiliary – platinum, using as supporting electrolyte 4.0 mL of Britton Robinson Buffer 0.04 mol L?1 (pH=4.0), 1.0 mL of methanol and 5.50×10?4 mol L?1 of cetyltrimethylammonium bromide (CTAB). The method was validated using three commercial sunscreen samples and the results showed recovery values between 83 and 98 %. The average values found for the analysed samples were 3.49 % m/m (728 mg L?1) to BZ‐3, 0.56 % m/m (113 mg L?1) to MBC and 0.99 % m/m (208 mg L?1) to OMC. The detection (DL) and quantification (QL) limits were 0.47 mg L?1 and 1.56 mg L?1 to BZ‐3, 0.77 mg L?1 and 2.58 mg L?1 to MBC and 0.78 mg L?1 and 2.59 mg L?1 to OMC, respectively. The sunscreen protector samples were also evaluated by high‐performance liquid chromatography (HPLC) demonstrating a good correlation between the results and compared the results with allowed concentration. 相似文献
957.
Arnaud Imberdis Guillaume Lefvre Thibault Cantat 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(48):17375-17379
The selective decarbonylation of formic acid was achieved under transition‐metal‐free conditions. Using a liquid chemical‐looping strategy, the thermodynamically favored dehydrogenation of formic acid was shut down, yielding a pure stream of CO with no H2 or CO2 contamination. The transformation involves a two‐step sequence where methanol is used as a recyclable looping agent to yield methylformate, which is subsequently decomposed to carbon monoxide using alkoxides as catalysts. 相似文献
958.
Yue Liu Mingxin Lv Lu Li Hailong Yu Qiong Wu Jinhui Pang Yuxiang Liu Congxia Xie Shitao Yu Shiwei Liu 《应用有机金属化学》2019,33(4)
An amino‐functionalized silica‐coated Fe3O4 nanocomposite (Fe3O4@SiO2/APTS) was synthesized. The Fe3O4@SiO2 microspheres possessed a well‐defined core–shell structure, uniform sizes and high magnetization. An immobilized ruthenium nanoparticle catalyst (Fe3O4@SiO2/APTS/Ru) was obtained after coordination and reduction of Ru3+ on the Fe3O4@SiO2/APTS nanocomposite. The Ru nanoparticles were not only ultra‐small with nearly monodisperse sizes but also had strong affinity with the surface of Fe3O4@SiO2/APTS. The obtained catalyst exhibited excellent catalytic performance for the hydrogenation of a variety of aromatic nitro compounds, even at room temperature. Moreover, Fe3O4@SiO2/APTS/Ru was easily recovered using a magnetic field and directly reused for at least five cycles without significant loss of its activity. 相似文献
959.
DAI Jianan LIU Bengen WEI Zhonglin CAO Jungang LIANG Dapeng DUAN Haifeng LIN Yingjie 《高等学校化学研究》2019,35(2):216-220
A straiglitforward and efficient synthetic method of 2′-(dialkylammo)-l-alkyl-4′H-spiro[indoline-3,5′-oxazole]-2,4′-diones and 2-(dialkylamino)-5,6-dihydro-4H-naphtho[2,1-e][1,3]oxazin-4-one-derivatives have been developed from a-hydroxy andβ-carbonyl amides and various Vilsmeier salts.A wide range of heterocyclic compounds were obtained in excellent yields(up to 97%),which will provide promising candidates lor chemical biology and drug discovery. 相似文献
960.
We developed a method for the simultaneous quantification of aceclofenac and its three major metabolites in rat plasma. After protein precipitation with acetonitrile including flufenamic acid as an internal standard (IS), aceclofenac, diclofenac, 4'-hydroxyaceclofenac, 4'-hydroxydiclofenac, and the IS were chromatographed on a reverse-phase C18 analytical column. The isocratic mobile phase of acetonitrile/0.1% formic acid (aq; 9:1 [v/v]) was eluted at 0.3 mL/min. Quantification was performed on a triple-quadrupole mass spectrometer using electrospray ionization, and the ion transitions were monitored in selective reaction-monitoring mode. The coefficient of variation in the assay precision was less than 8%, and the accuracy was 92-103%. This method was successfully used to measure the concentrations of aceclofenac and its three major metabolites in rat plasma following the oral administration of a single 20 mg/kg oral dose of aceclofenac. 相似文献