全文获取类型
收费全文 | 395篇 |
免费 | 14篇 |
国内免费 | 1篇 |
专业分类
化学 | 333篇 |
晶体学 | 2篇 |
力学 | 2篇 |
数学 | 18篇 |
物理学 | 55篇 |
出版年
2023年 | 3篇 |
2022年 | 4篇 |
2021年 | 3篇 |
2020年 | 2篇 |
2019年 | 9篇 |
2018年 | 6篇 |
2017年 | 3篇 |
2016年 | 8篇 |
2015年 | 4篇 |
2014年 | 7篇 |
2013年 | 17篇 |
2012年 | 23篇 |
2011年 | 24篇 |
2010年 | 16篇 |
2009年 | 16篇 |
2008年 | 24篇 |
2007年 | 24篇 |
2006年 | 24篇 |
2005年 | 23篇 |
2004年 | 16篇 |
2003年 | 18篇 |
2002年 | 17篇 |
2001年 | 15篇 |
2000年 | 19篇 |
1999年 | 2篇 |
1998年 | 5篇 |
1995年 | 4篇 |
1994年 | 3篇 |
1993年 | 2篇 |
1992年 | 4篇 |
1991年 | 2篇 |
1990年 | 4篇 |
1989年 | 5篇 |
1988年 | 3篇 |
1986年 | 3篇 |
1985年 | 3篇 |
1984年 | 5篇 |
1983年 | 3篇 |
1982年 | 2篇 |
1981年 | 3篇 |
1979年 | 6篇 |
1978年 | 2篇 |
1977年 | 3篇 |
1976年 | 3篇 |
1975年 | 2篇 |
1974年 | 4篇 |
1973年 | 3篇 |
1972年 | 3篇 |
1968年 | 1篇 |
1967年 | 1篇 |
排序方式: 共有410条查询结果,搜索用时 15 毫秒
1.
Ryoko Chiba Ayako Ogasawara Teppei Kubo Hiroyuki Yamazaki Masuo Umino Yoichi Ishizuka 《Analytical sciences》2003,19(5):785-789
A column-switching high-performance liquid chromatographic method with fluorescence detection was developed for the simultaneous determination of four benzamide-type anti-psychotic drugs: sulpiride, tiapride, sultopride and metoclopramide in human serum. In this method, a TSKgel Super-ODS column was used as an analytical column, and a TSKgel G 2000SW was prepared as a pretreatment column. Under the optimized analytical conditions, four benzamide-type anti-psychotic drugs were eluted within 18 min. The detection limits (S/N = 3) for sulpiride, tiapride, sultopride and metoclopramide are 1 ng/ml, 4 ng/ml, 2 ng/ml and 0.5 ng/ml, respectively. Finally, the method was applied to the determination of sulpiride in human serum samples obtained after a single oral dose of sulpiride. 相似文献
2.
A concise route to (-)-kainic acid from enantiopure (+)-cis-4-carbobenzoxyamino-2-cyclopentenol has been devised by employing concurrent Chugaev syn-elimination and intramolecular ene reaction as the key step. 相似文献
3.
4.
5.
The (132R)-methoxycarbonyl group of methyl pheophorbide a, one of the chlorophyll-a derivatives, was converted to a methyl group through methylation at the C132 position followed by removal of the methoxycarbonyl group. The methylation of the C132 carboanion gave a 4:1 mixture of methyl 132-methyl-pheophorbide a and its 132-epimer. The successive pyrolysis of the major methylated product afforded methyl (132R)-methyl-pyropheophorbide a with a small amount of its (132S)-epimer. The substitution effects at the C132 position including stereochemistry were discussed on the basis of 1D/2D NMR, UV–vis absorption, and circular dichroism spectroscopic analyses as well as molecular modeling simulation. 相似文献
6.
Chie Hosokawa Yasutaka Sakamoto Suguru N. Kudoh Yoichiroh Hosokawa Takahisa Taguchi 《Applied Physics A: Materials Science & Processing》2013,110(3):607-612
We demonstrated the stimulation of neurons at a single-cell level in cultured neuronal network by a focused femtosecond laser. When the femtosecond laser was focused on a neuron loaded with a fluorescent calcium indicator, the fluorescence intensity immediately increased at the laser spot, suggesting that intracellular Ca2+ increases in the neuronal cell due to the femtosecond laser irradiation. The probability of Ca2+ elevation at the laser spot depended on the average laser power, irradiation time, and position of the focal point along the optical axis, indicating that the femtosecond laser activates neurons because of multiphoton absorption. Moreover, after laser irradiation of a single neuron cultured on multielectrode arrays, the evoked electrical activity of the neurons was demonstrated by electrophysiological systems, which concluded that the focused femtosecond laser could achieve stimulating a single neuron in a neuronal network with high spatial and temporal resolution. 相似文献
7.
Atsunori Ono Yohei Takahashi Sumio Kato Masataka Ogasawara Takashi Wakabayashi Yuunosuke Nakahara Shinichi Nakata 《Research on Chemical Intermediates》2011,37(9):1225-1230
A10(PO4)6(OH)2 (A = Ca and Sr)-supported Pt catalysts were prepared and their catalytic activity in NO reduction were investigated. The Sr10(PO4)6(OH)2-supported catalyst had high catalytic activity in the C3H6?CNO?CO2 reaction; the activity was higher than that of the ??-Al2O3-supported catalyst at 300 °C. The basicity of the apatite supports would affect the chemical state of Pt on catalyst, resulting in promotion of NO reduction. 相似文献
8.
Uchida S Kamata K Ogasawara Y Fujita M Mizuno N 《Dalton transactions (Cambridge, England : 2003)》2012,41(33):9979-9983
The structural and dynamical aspects of alkylammonium salts of a silicodecatungstate [(CH(3))(4)N](4)[γ-SiW(10)O(34)(H(2)O)(2)] [C1], [(n-C(3)H(7))(4)N](4)[γ-SiW(10)O(34)(H(2)O)(2)] [C3], [(n-C(4)H(9))(4)N](4)[γ-SiW(10)O(34)(H(2)O)(2)] [C4], and [(n-C(5)H(11))(4)N](4)[γ-SiW(10)O(34)(H(2)O)(2)] [C5] were investigated. The results of sorption isotherms, XRD analyses, and solid-state NMR spectroscopy show that facile sorption of solvent molecules, flexibility of structures, and high mobility of alkylammonium cations are crucial to the uniform distribution of reactant and oxidant molecules throughout the bulk solid, which are related to the high catalytic activities for epoxidation of alkenes. 相似文献
9.
[reaction: see text] A three-step route of converting allylsilanes to functionalized allenes was developed. Thermal decomposition of 1,1-dibromo-2-(silylmethyl)cyclopropanes, which were quantitatively prepared by treatment of allylsilane derivatives with CHBr3/KO(t)Bu, afforded substituted 2-bromo-1,3-butadienes with elimination of bromosilanes. The Pd-catalyzed reaction of the bromodienes with soft nucleophiles gave the allene derivatives. Previously inaccessible tri- and tetrasubstituted allenes can be prepared by this method as well. 相似文献
10.
Shunsuke Kotani Masaya Ito Hirono Nozaki Masaharu Sugiura Masamichi Ogasawara Makoto Nakajima 《Tetrahedron letters》2013
An application of a hypervalent silicon complex, generated from a chiral phosphine oxide catalyst and silicon tetrachloride, to the enantioselective organocatalytic Morita–Baylis–Hillman reaction is described. A chloride anion liberated from the hypervalent silicon complex smoothly generated a γ-chloro silyl enol ether that subsequently reacted with an aldehyde to afford the Baylis–Hillman adducts in good yields and with good enantioselectivities. 相似文献