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101.
《Electroanalysis》2017,29(4):1188-1196
In this work, one novel electrochemical sensor was prepared by alternative deposition of phosphomolybdic acid (PMoA) and poly(ethyleneimine) (PEI) on an indium tin oxide glass substrate through layer‐by‐layer assembly. The performance of as‐prepared electrode was evaluated with both of oxidizing compounds of iodate and H2O2 and reducing compounds of dopamine and ascorbic acid as models. The results showed that corresponding current response of redox peak increased linearly with the concentration of above compounds increasing in certain ranges, respectively. Limits of detection to them were in the range of 1.0×10−4 ‐ 4.3×10−4 mg mL−1 with cyclic voltammetry (CV) in 0.1 mol L−1 NaAc‐HAc buffer (pH 5.0). The electrode showed high stability and remained 95 % of its initial activity even after 100 cycles of CV scan. When applied in real samples of table salts, juice and human serum, high recoveries of 96.84 to 100.33 % were achieved with relative standard deviations of 1.11‐3.96 % (n=3) at three spiked levels. Moreover, it was also successfully applied for the simultaneous determination of dopamine and ascorbic acid in human serum with differential pulse voltammetry. The results indicated that PMoA/PEI multilayer modified electrode can be used as a universal electrochemical sensor for sensitive detection of redox compounds. 相似文献
102.
ABSTRACTA repeat unit of cell wall teichoic acids (WTA) isolated from E. faecium U0317 was chemically synthesized efficiently by a stepwise strategy. It was derivatized with a 5-aminopentanyl linker to facilitate conjugation with carrier proteins KLH and HSA. Immunological studies of the KLH conjugate 1 demonstrated that it could provoke robust immune responses and high titers of IgG antibodies, which could successfully recognize the synthesized WTA repeat unit 3. This result suggested that synthetic glycoconjugate 1 could be a promising vaccine candidate against E. faecium for further studies. 相似文献
103.
Santosh Ramdas Borkar Naveen Bokolia Indrapal Singh Aidhen Inshad Ali Khan 《Tetrahedron: Asymmetry》2017,28(1):186-195
A series of threo- and erythro-configured open-chain trihydroxy ketones was synthesized starting from l- and d-ascorbic acid respectively as the starting material, through the use of Grignard reactions for the requisite CC bond formations. The lipophilic ketones were screened against Mycobacteriumtuberculosis for anti-proliferative activity. The lipophilic ketones with tetradecyl alkyl side chains were found to be moderately active against cell proliferation. 相似文献
104.
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107.
主要以两不同型部件组成的并联可修系统为研究对象.在系统对失效相位存在记忆的基础上,考虑了修理工可单重休假且休假时间服从位相(PH)分布.每个工作部件均有可能因受到两种不同类型的故障而失效,且均"修复非新".在假定部件的工作时间,修理时间分别服从PH分布的几何过程和负指数分布的条件下,利用马尔可夫过程和矩阵分析的方法,对可修系统进行了可靠性分析,并给出了相应可靠性指标的数值算例. 相似文献
108.
Recently developed strategies for late stage modification of peptides through CH activation, an arena of contemporary interest in chemical biology and drug discovery, are discussed. Through this tactic, non-polar amino acids in peptides have been selectively functionalized and CH activation enabled new CC and CX bond formations (arylation, alkynylation, fluorination, hydroxylation, azidation, etc.) are documented. Significant advances have been made in Pd or Au-catalyzed, racemization-free, tryptophan specific modifications of large peptides via CH arylation and alkynylation reactions without any protecting group requirement. Development of a new biaryl stapling technique for complex peptides, 18F radiofluorine introduction and diversity oriented post synthetic applications on bio-active cyclopeptides like valinomycin and aureobasidin are additional highlights which underscores the vast potential of late stage CH activation reactions in peptide based therapeutics research. 相似文献
109.
An iodine-catalyzed aerobic-oxidative C-H functionalization of o-alkylazoarenes to afford 2H-indazoles has been developed. CuI was found to be an effective additive to accelerate the regeneration of iodine in the catalytic cycle. This catalytic system is suitable for both electron-rich and electron-deficient azoarenes and tolerates a variety of functional groups with high yields. A gram-scale reaction was successfully conducted, proving the scalability of this reaction. 相似文献
110.
Antonín Klásek Filip Křemen Hana Křemenová Antonín Lyčka Michal Rouchal 《Tetrahedron》2017,73(12):1583-1593
The reaction of tertiary α-chloroketones with ethanolamine has not been hitherto described in the literature. Herein, we describe the reaction of tertiary 3-chloroquinoline-2,4-diones with ethanolamine to give novel 3-(2-hydroxyethylamino)quinoline-2,4-diones. These compounds provide 3-(2-oxooxazolidin-3-yl)quinoline-2,4(1H,3H)-diones and new compounds with dimeric character after reaction with triphosgene. Molecular rearrangement proceeds during the reaction of 3-(2-hydroxyethylamino)quinoline-2,4-diones with isocyanic acid. Three types of reaction products arise: 2-(2-hydroxyethyl)imidazo[1,5-c]quinazoline-3,5-diones, 3-(2-hydroxyethyl)-3,3a-dihydro-2H-imidazo[4,5-]quinoline-4(5H)diones and primarily 5-hydroxy-1-(hydroxyethyl)-1′H-spiro[imidazolidine-5,3′-indole]-2,2′-diones. The reaction mechanism and product stereochemistry are discussed. The 1H, 13C and 15N NMR spectra of the prepared compounds were measured, and all resonances were assigned from appropriate two-dimensional experiments. 相似文献