全文获取类型
收费全文 | 2281篇 |
免费 | 72篇 |
国内免费 | 5篇 |
专业分类
化学 | 1753篇 |
晶体学 | 4篇 |
力学 | 18篇 |
数学 | 341篇 |
物理学 | 242篇 |
出版年
2023年 | 29篇 |
2022年 | 20篇 |
2021年 | 26篇 |
2020年 | 64篇 |
2019年 | 53篇 |
2018年 | 30篇 |
2017年 | 19篇 |
2016年 | 44篇 |
2015年 | 31篇 |
2014年 | 42篇 |
2013年 | 70篇 |
2012年 | 74篇 |
2011年 | 105篇 |
2010年 | 43篇 |
2009年 | 50篇 |
2008年 | 74篇 |
2007年 | 70篇 |
2006年 | 75篇 |
2005年 | 73篇 |
2004年 | 66篇 |
2003年 | 48篇 |
2002年 | 44篇 |
2001年 | 20篇 |
2000年 | 27篇 |
1999年 | 15篇 |
1998年 | 18篇 |
1996年 | 15篇 |
1995年 | 21篇 |
1994年 | 20篇 |
1991年 | 21篇 |
1990年 | 15篇 |
1988年 | 15篇 |
1987年 | 15篇 |
1986年 | 17篇 |
1985年 | 27篇 |
1984年 | 31篇 |
1983年 | 25篇 |
1982年 | 41篇 |
1981年 | 24篇 |
1980年 | 26篇 |
1979年 | 45篇 |
1978年 | 25篇 |
1977年 | 37篇 |
1976年 | 28篇 |
1975年 | 24篇 |
1974年 | 20篇 |
1973年 | 17篇 |
1967年 | 19篇 |
1956年 | 20篇 |
1934年 | 23篇 |
排序方式: 共有2358条查询结果,搜索用时 31 毫秒
1.
A profit-maximizing supply chain network design model with demand choice flexibility 总被引:1,自引:0,他引:1
Zuo-Jun Max Shen 《Operations Research Letters》2006,34(6):673-682
We present a profit-maximizing supply chain design model in which a company has flexibility in determining which customers to serve. The company may lose a customer to competition if the price it charges is too high. We show the problem formulation and solution algorithm, and discuss computational results. 相似文献
2.
In this Note, we give a necessary and sufficient condition for Lagrangians in a symplectic vector bundle to be deformed stably into transversal Lagrangians. In the case of three Lagrangians, we show that the associated Grothendieck group can be identified with a Hermitian K-theory group. To cite this article: M. Karoubi, M.L. Lapa de Souza, C. R. Acad. Sci. Paris, Ser. I 342 (2006). 相似文献
3.
Vicenç Branchadell Roser Pleixats Claude Commandeur Max Malacria 《Journal of organometallic chemistry》2003,687(2):337-345
Regioselectivity of the Tsuji-Trost reaction on allyl acetates and carbonates substituted with silyl groups at the olefinic moiety has been analyzed. Silicon atom in the central carbon atom increases the stability of the intermediate π-allylpalladium cation with respect to the isomeric π-allylpalladium cation featuring the silicon in a terminal carbon atom. 相似文献
4.
5.
A stable model category is a setting for homotopy theory where the suspension functor is invertible. The prototypical examples are the category of spectra in the sense of stable homotopy theory and the category of unbounded chain complexes of modules over a ring. In this paper we develop methods for deciding when two stable model categories represent ‘the same homotopy theory’. We show that stable model categories with a single compact generator are equivalent to modules over a ring spectrum. More generally stable model categories with a set of generators are characterized as modules over a ‘ring spectrum with several objects’, i.e., as spectrum valued diagram categories. We also prove a Morita theorem which shows how equivalences between module categories over ring spectra can be realized by smashing with a pair of bimodules. Finally, we characterize stable model categories which represent the derived category of a ring. This is a slight generalization of Rickard's work on derived equivalent rings. We also include a proof of the model category equivalence of modules over the Eilenberg-Mac Lane spectrum HR and (unbounded) chain complexes of R-modules for a ring R. 相似文献
6.
7.
Diemar A. Plattner Andreas Brunner Max Dobler Hans-Martin Müller Walter Petter Peter Zbinden Dieter Seebach 《Helvetica chimica acta》1993,76(5):2004-2033
Cyclic Oligomers of (R)-3-Hydroxybutanoic Acid: Preparation and Structural Aspects The oligolides containing three to ten (R)-3-hydroxybutanoate (3-HB) units (12-through 40-membered rings 1–8 ) are prepared from the hydroxy acid itself, its methyl ester, its lactone (‘monolide’), or its polymer (poly(3-HB), mol. wt. ca. 106 Dalton) under three sets of conditions: (i) treatment of 3-HB ( 10 ) with 2,6-dichlorobenzoyl chloride/pyridine and macrolactonization under high dilution in toluene with 4-(dimethylamino)pyridine (Fig. 3); (ii) heating a solution (benzene, xylene) of the β-lactone 12 or of the methyl ester 13 from 3-HB with the tetraoxadistanna compound 11 as trans-esterification catalyst (Fig. 4); (iii) heating a mixture of poly(3-HB) and toluene-sulfonic acid in toluene/1,2-dichloroethane for prolonged periods of time at ca. 100° (Fig. 6). In all three cases, mixtures of oligolides are formed with the triolide 1 being the prevailing component (up to 50% yield) at higher temperatures and with longer reaction times (thermodynamic control, Figs. 3–6). Starting from rac-β-lactone rac- 12 , a separable 3:1 to 3:2 mixture of the l,u- and the l,l-triolide diasteroisomers rac- 14 and rac- 1 , respectively, is obtained. An alternative method for the synthesis of the octolide 6 is also described: starting from the appropriate esters 15 and 17 and the benzyl ether 16 of 3-HB, linear dimer, tetramer, and octamer derivatives 18–23 are prepared, and the octamer 23 with free OH and CO2H group is cyclized (→ 6 ) under typical macrolactonization conditions (see Scheme). This ‘exponential fragment coupling protocol’ can be used to make higher linear oligomers as well. The oligolides 1–8 are isolated in pure form by vacuum distillation, chromatography, and crystallization, an important analytical tool for determining the composition of mixtures being 13C-NMR spectroscopy (each oligolide has a unique and characteristic chemical shift of the carbonyl C-atom, with the triolide 1 at lowest, the decolide 8 at highest field). The previously published X-ray crystal structures of triolide 1 , pentolide 3 , and hexolide 4 (two forms), as well as those of the l,u-triolide rac- 14 , of tetrolide ent- 2 , of heptolide 5 , and of two modifications of octolide 6 described herein for the first time are compared with each other (Figs. 7–10 and 12–15, Tables 2 and 5–7) and with recently modelled structures (Tables 3 and 4, Fig. 11). The preferred dihedral angles τ1 to τ4 found along the backbone of the nine oligolide structures (the hexamer and the larger ones all have folded rings!) are mapped and statistically evaluated (Fig. 16, Tables 5–7). Due to the occurrence of two conformational minima of the dihedral angle O? CO? CH2? CH (τ3 = + 151 or ?43°), it is possible to locate two types of building blocks for helices in the structures at hand: a right-handed 31 and a left-handed 21 helix; both have a ca. 6 Å pitch, but very different shapes and dispositions of the carbonyl groups (Fig. 17). The 21 helix thus constructed from the oligolide single-crystal data is essentially superimposable with the helix derived for the crystalline domains of poly(3-HB) from stretched-fiber X-ray diffraction studies. The absence of the unfavorable (E)-type arrangements around the OC? OR bond (‘cis-ester’) from all the structures of (3-HB) oligomers known so far suggests that the model proposed for a poly(3-HB)-containing ion channel (Fig. 2) must be modified. 相似文献
8.
9.
10.