全文获取类型
收费全文 | 1050篇 |
免费 | 80篇 |
国内免费 | 1篇 |
专业分类
化学 | 934篇 |
力学 | 6篇 |
数学 | 59篇 |
物理学 | 132篇 |
出版年
2023年 | 14篇 |
2022年 | 33篇 |
2021年 | 47篇 |
2020年 | 41篇 |
2019年 | 47篇 |
2018年 | 21篇 |
2017年 | 20篇 |
2016年 | 56篇 |
2015年 | 55篇 |
2014年 | 39篇 |
2013年 | 64篇 |
2012年 | 92篇 |
2011年 | 113篇 |
2010年 | 69篇 |
2009年 | 30篇 |
2008年 | 65篇 |
2007年 | 78篇 |
2006年 | 53篇 |
2005年 | 52篇 |
2004年 | 32篇 |
2003年 | 32篇 |
2002年 | 22篇 |
2001年 | 11篇 |
2000年 | 2篇 |
1999年 | 6篇 |
1996年 | 5篇 |
1995年 | 2篇 |
1994年 | 4篇 |
1993年 | 4篇 |
1992年 | 5篇 |
1991年 | 2篇 |
1990年 | 2篇 |
1989年 | 1篇 |
1987年 | 2篇 |
1984年 | 1篇 |
1982年 | 2篇 |
1979年 | 2篇 |
1978年 | 1篇 |
1975年 | 1篇 |
1974年 | 1篇 |
1968年 | 1篇 |
1965年 | 1篇 |
排序方式: 共有1131条查询结果,搜索用时 15 毫秒
41.
Jessica Silva Joo Basso Joo Sousa Ana Fortuna Carla Vitorino 《Biomedical chromatography : BMC》2019,33(10)
There is increasing interest in atorvastatin and curcumin owing to their potential anticancer activity. A new, accurate and sensitive HPLC method was developed, for the first time, to simultaneously quantify atorvastatin and curcumin in mouse plasma and brain, liver, lung and spleen tissues following protein precipitation sample preparation. The chromatographic separation was achieved in 13 min on a C18 column, at 35°C, using a mobile phase composed of acetonitrile–methanol–2% (v/v) acetic acid (37.5:2.5:60, v/v/v) at a flow rate of 1.0 mL/min. The detection of analytes and internal standard was carried out at 247, 425 and 250 nm, respectively. According to international guidelines, the method was shown to be selective, with lower limits of quantification ranging from 10 to 500 ng/mL for curcumin, and from 100 to 600 ng/mL for atorvastatin, linear over a wide concentration range (r2 ≥ 0.9971) and with acceptable accuracy (bias ± 12.29%) and precision (coefficient of variation ≤13.15%). The analytes were reproducibly recovered at a percentage >81.10% and demonstrated to be stable under various experimental conditions in all biological matrices. This method can be easily applied to in vivo biodistribution studies related to the intranasal administration of atorvastatin and curcumin, separately or simultaneously. 相似文献
42.
43.
Dr. Jessica Rodríguez Dr. Miguel Martínez-Calvo 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(44):9792-9813
The site-selective modification of biomolecules has grown spectacularly in recent years. The presence of a large number of functional groups in a biomolecule makes its chemo- and regioselective modification a challenging goal. In this context, transition-metal-mediated reactions are emerging as a powerful tool owing to their unique reactivity and good functional group compatibility, allowing highly efficient and selective bioconjugation reactions that operate under mild conditions. This Minireview focuses on the current state of organometallic chemistry for bioconjugation, highlighting the potential of transition metals for the development of chemoselective and site-specific methods for functionalization of peptides, proteins and nucleic acids. The importance of the selection of ligands attached to the transition metal for conferring the desired chemoselectivity will be highlighted. 相似文献
44.
Messenger RNA (mRNA)-based vaccines are advantageous because they can be relatively quicker and more cost efficient to manufacture compared to other traditional vaccine products. Lipid nanoparticles have three common purposes: delivery, self-adjuvanting properties, and mRNA protection. Faster vaccine development requires an efficient and fast assay to monitor mRNA purity and integrity. Microchip CE is known to be a robust technology that is capable of rapid separation. Here, we describe the development and optimization of a purity and integrity assay for mRNA-based vaccines encapsulated in lipid nanoparticles using commercial microchip-based separation. The analytical parameters of the optimized assay were assessed and the method is a stability indicating assay. 相似文献
45.
Measure-free discrete time stochastic processes in Riesz spaces were formulated and studied by Kuo, Labuschagne and Watson. Aspects relating martingales, stopping times, convergence of these processes as well as various decomposition were considered. Here we formulate and study Markov processes in a measure-free Riesz space setting. 相似文献
46.
47.
Richard A. Bunce James E. Schammerhorn Jessica Sigle 《Journal of heterocyclic chemistry》2013,50(2):373-380
A tandem imine addition‐SNAr annulation reaction has been developed as a new approach to the synthesis of 4‐oxo‐1,2,3,4‐tetrahydroquinoline‐3‐carboxylic esters. A series of these structures has been generated by reacting selected imines with tert‐butyl 2‐fluoro‐5‐nitrobenzoylacetate. Structural variations in the final products are accomplished by changing the substituents on the imine and the alkyl group of the ester. The title compounds are isolated as their enols in 55–97% yield without the need for added base or catalysts. The synthesis of the starting materials as well as mechanistic studies and further synthetic conversions of the products are presented. 相似文献
48.
This report describes the synthesis of 4‐substituted‐ and 1,4‐disubstituted‐4‐hydroxypyrrolidin‐2‐ones by cyclization of intermediate γ‐aminoesters prepared from alkylbenzylamines, α‐bromoketones, and lithio ethyl acetate. 相似文献
49.
1,4-Diazabicyclo[2.2.2]octane (DABCO) has been used as a mild and efficient catalyst for the synthesis of various tetrahydrobenzo[b]pyran derivatives via a one-pot, three component condensation of aromatic aldehydes, dimedone, and active methylene compounds. This method provides several advantages: a simple workup procedure, environmental friendliness, neutral conditions, and good yields. In addition, water or 50% aqueous ethanol was chosen as a green solvent.
50.
Markus R. Meyer Carina Lindauer Jessica Welter Hans H. Maurer 《Analytical and bioanalytical chemistry》2014,406(7):1845-1854
Dimethocaine (DMC, larocaine), a synthetic derivative of cocaine, is a widely distributed “legal high” consumed as a “new psychoactive substance” (NPS) without any safety testing, for example studies of metabolism. Therefore, the purpose of this work was to study its in-vivo and in-vitro metabolism by use of liquid chromatography–(high resolution) mass spectrometry (LC–HRMS n ). DMC was administered to male Wistar rats (20 mg kg?1) and their urine was extracted either by solid-phase extraction after enzymatic cleavage of conjugates or by use of protein precipitation (PP). The metabolites were separated and identified by LC–HRMS n . The main phase I reactions were ester hydrolysis, deethylation, hydroxylation of the aromatic system, and a combination of these. The main phase II reaction was N-acetylation of the p-aminobenzoic acid part of the unchanged parent compound and of several phase I metabolites. The metabolites identified were then used for identification of DMC in rat urine after application of a common user’s dose. By use of GC–MS and LC–MS n standard urine-screening approaches (SUSAs), DMC and its metabolites could be detected in the urine samples. 相似文献