全文获取类型
收费全文 | 7857篇 |
免费 | 1389篇 |
国内免费 | 829篇 |
专业分类
化学 | 5834篇 |
晶体学 | 12篇 |
力学 | 916篇 |
综合类 | 52篇 |
数学 | 2144篇 |
物理学 | 1117篇 |
出版年
2024年 | 6篇 |
2023年 | 98篇 |
2022年 | 155篇 |
2021年 | 203篇 |
2020年 | 390篇 |
2019年 | 215篇 |
2018年 | 269篇 |
2017年 | 233篇 |
2016年 | 373篇 |
2015年 | 447篇 |
2014年 | 475篇 |
2013年 | 678篇 |
2012年 | 523篇 |
2011年 | 551篇 |
2010年 | 492篇 |
2009年 | 554篇 |
2008年 | 592篇 |
2007年 | 527篇 |
2006年 | 495篇 |
2005年 | 455篇 |
2004年 | 406篇 |
2003年 | 467篇 |
2002年 | 179篇 |
2001年 | 188篇 |
2000年 | 175篇 |
1999年 | 139篇 |
1998年 | 134篇 |
1997年 | 131篇 |
1996年 | 125篇 |
1995年 | 84篇 |
1994年 | 65篇 |
1993年 | 43篇 |
1992年 | 53篇 |
1991年 | 37篇 |
1990年 | 26篇 |
1989年 | 22篇 |
1988年 | 8篇 |
1987年 | 12篇 |
1986年 | 7篇 |
1985年 | 11篇 |
1984年 | 9篇 |
1983年 | 7篇 |
1982年 | 3篇 |
1981年 | 1篇 |
1980年 | 4篇 |
1979年 | 2篇 |
1978年 | 2篇 |
1976年 | 2篇 |
1957年 | 1篇 |
1936年 | 1篇 |
排序方式: 共有10000条查询结果,搜索用时 31 毫秒
121.
针对现有船舶过闸排队规则的欠缺,基于“限时服务规则”,构建复线船闸多目标双层优化调度模型:上层模型用于获得两个闸室安全区域的船舶排布可行方案;下层模型用于获得不同船舶排布可行方案的优化闸次数。下层模型分两个阶段完成:对符合“限时服务规则”的船舶,构建以闸次最少为目标的0-1规划模型,获得此类船舶安排的闸次;对其余船舶按照“先到先服务规则”,构建以闸次最少、闸室利用率最大为目标的多目标决策模型,获得不同船舶排布可行方案应该安排的频次。以位于江苏省干线航道上的某复线船闸某日24小时内过闸船舶的数据为例,计算结果表明:采用本文优化模型获得的优化方案与“经验编排方式”相比,两座船闸各节约2个闸次,两个船闸的平均闸室利用率分别提高了3.66和4.72个百分点。 相似文献
122.
This paper focus on the event-triggered sliding mode controller design for discrete-time switched genetic regulatory networks (GRNs) with persistent dwell time (PDT) switching. Firstly, the observation error dynamics of switched GRNs with PDT is constructed in the light of event-triggered sliding mode control (SMC) scheme. Next, sufficient conditions are derived to ensure the exponential stability of the augmented plant. Moreover, an event-triggered SMC law is synthesized to impel the system trajectories onto the sliding surface in a finite time. Finally, a verification example is provided to illustrate the effectiveness and potential of the proposed method. 相似文献
123.
Yu Chen 《Transactions of the American Mathematical Society》1996,348(9):3733-3743
We demonstrate a one to one correspondence between the irreducible projective representations of an affine Kac-Moody group and those of the related loop group, which leads to the results that every non-trivial representation of an affine Kac-Moody group must have its degree greater than or equal to the rank of the group and that the equivalence appears if and only if the group is of type for some . Moreover the characteristics of the base fields for the non-trivial representations are found being always zero.
124.
Yuri N. Belokon’Devayani Bhave Daniela D'AddarioElizabetta Groaz Viktor MaleevMichael North Armine Pertrosyan 《Tetrahedron letters》2003,44(10):2045-2048
Copper(salen) complex 1 has been found to catalyse the asymmetric alkylation of enolates derived from a variety of amino acids. There is a clear relationship between the size of the side chain in the substrate and the enantioselectivity of the process, so that the enantioselectivity decreases in the order alanine>aminobutyric acid>allylglycine>leucine>phenylalanine>valine. A transition state model which accounts for the influence of the size of the side chain on the enantioselectivity of the reactions is presented. 相似文献
125.
126.
Alcaide B Almendros P Alonso JM Aly MF 《Chemistry (Weinheim an der Bergstrasse, Germany)》2003,9(14):3415-3426
Imines derived from 4-oxoazetidine-2-carbaldehydes have been found to be versatile Diels-Alder reagents in that they exhibit two reactivity patterns. 2-Azetidinone-tethered imines undergo diastereoselective reaction with Danishefsky's diene in the presence of different Lewis acids. The effect of the amount of catalyst on the conversion rate as well as on the product ratio has been studied. Under standard reaction conditions, indium(III) chloride and zinc(II) iodide provided the best yields, and indium(III) triflate the highest diastereoselectivity in the Lewis acid promoted aza-Diels-Alder cycloaddition. Treatment of the aforementioned imines with cyclopentadiene, 2,3-dimethyl-1,3-butadiene or 3,4-dihydro-2 H-pyran led to cycloadducts arising from inverse electron-demand condensation involving the beta-lactam-tethered aryl imine as the heterodiene component. In addition, the first methodology for preparing indolizidines from beta-lactams has been developed. This process involves amide bond cleavage of the beta-lactam ring in the aza-Diels-Alder cycloadducts with concomitant cyclization. Full chirality transfer occurs when the reaction is performed with an enantiomerically pure substrate. 相似文献
127.
Y. E. Kuznetsov N. L. Sukhov F. V. Pichugin B. G. Ershov 《Russian Chemical Bulletin》1996,45(12):2816-2819
Reactions ofmyo-inositiol hexa-O-nitrate with ammonia and primary amines yield tetrahydroxy-1,4-benzoquinone derivatives,viz., its tetraammonium salt and its diimines, respectively. Reactions with secondary and tertiary amines give salts of rhodizonic acid, which are converted into salts of croconic acid under certain conditions. The reactions with secondary amines involve intermediate formation of radical species, which were dectected by ESR spectroscopy. A scheme for the chemical transformations ofmyo-inositol hexa-O-nitrate under the action of amines was proposed.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 12, pp. 2962–2967, December, 1996. 相似文献
128.
The rare earth(III) salt catalysed asymmetric Diels–Alder reaction of cyclopentadiene with a chiral dienophile in supercritical carbon dioxide (scCO2) proceeded rapidly to give the adduct with a higher diastereoselectivity than that in dichloromethane; Yb(ClO4)3 gave the endo adduct with value up to 77% de at 40°C, 8 MPa. The chiral rare earth diketonate catalyzed hetero Diels–Alder reaction of the Danishefsky's diene with benzaldehyde gave a higher yield and an enantioselectivity in scCO2 than that in dichloromethane. Scandium/pybox 8a complex catalysed asymmetric Diels–Alder reaction of 3-crotonoyl-2-oxazolidinone with cyclopentadiene in the presence of MS4A proceeded smoothly in scCO2 to give the endo adduct 10 in a good yield with up to 88% ee. 相似文献
129.
A convergent selective route to (+)-brefeldin A (BFA) and 7-epi-BFA was developed, with the crucial C-4/C-5 stereogenic centers were established using Crimmins asymmetric aldolization. 相似文献
130.