全文获取类型
收费全文 | 2452篇 |
免费 | 46篇 |
国内免费 | 9篇 |
专业分类
化学 | 1842篇 |
晶体学 | 67篇 |
力学 | 45篇 |
数学 | 66篇 |
物理学 | 487篇 |
出版年
2023年 | 12篇 |
2022年 | 19篇 |
2021年 | 22篇 |
2020年 | 27篇 |
2019年 | 28篇 |
2018年 | 18篇 |
2016年 | 38篇 |
2015年 | 49篇 |
2014年 | 46篇 |
2013年 | 116篇 |
2012年 | 105篇 |
2011年 | 111篇 |
2010年 | 65篇 |
2009年 | 69篇 |
2008年 | 112篇 |
2007年 | 136篇 |
2006年 | 140篇 |
2005年 | 120篇 |
2004年 | 124篇 |
2003年 | 100篇 |
2002年 | 103篇 |
2001年 | 84篇 |
2000年 | 68篇 |
1999年 | 40篇 |
1998年 | 29篇 |
1997年 | 21篇 |
1996年 | 34篇 |
1995年 | 34篇 |
1994年 | 30篇 |
1993年 | 31篇 |
1992年 | 63篇 |
1991年 | 28篇 |
1990年 | 28篇 |
1989年 | 26篇 |
1988年 | 28篇 |
1987年 | 32篇 |
1986年 | 33篇 |
1985年 | 28篇 |
1984年 | 38篇 |
1983年 | 19篇 |
1982年 | 18篇 |
1981年 | 19篇 |
1980年 | 18篇 |
1979年 | 28篇 |
1978年 | 22篇 |
1977年 | 18篇 |
1976年 | 20篇 |
1975年 | 13篇 |
1974年 | 22篇 |
1973年 | 13篇 |
排序方式: 共有2507条查询结果,搜索用时 0 毫秒
61.
Glycosides of benzyl and salicyl alcohols from Alangium chinense 总被引:1,自引:0,他引:1
Itoh A Tanahashi T Nagakura N Inoue K Kuwajima H Wu HX 《Chemical & pharmaceutical bulletin》2001,49(10):1343-1345
From the water-soluble fraction of the dried leaves of Alangium chinense, three new glycosides, benzyl alcohol beta-D-glucopyranosyl-(1 --> 2)-[beta-D-xylopyranosyl-(1 --> 6)]-beta-D-glucopyranoside, 2'-O-beta-D-glucopyranosylsalicin, and 2'-O-beta-D-glucopyranosyl-6'-O-beta-D-xylopyranosylsalicin were isolated along with seven known glycosides. The structures of the new compounds were determined by spectroscopic and chemical means. 相似文献
62.
Two new flavonol glycosides were isolated together with two known glycosides and an ester from the leaves of E. lanceollata Warb. Their structures were characterized by spectroscopic methods. 相似文献
63.
64.
1,2- Or 1,3-asymmetric induction in the iodocarbocyclization reaction of 4-pentenylmalonate derivatives having a stereogenic center at an allylic or a homoallylic position has been investigated. The iodocarbocyclization reactions of 3-oxy-4-pentenylmalonate derivatives proceeded with high cis-selectivity through stereoelectronic control of the oxygenated substituent at an allylic position. In the reaction of (S)-2-siloxy-4-pentenylmalonate, an excellent diastereoselectivity was achieved through the utilization of double stereodifferentiation with a chiral titanium catalyst. Furthermore, as an application of the present reaction, the asymmetric syntheses of cyclosarkomycin and a synthetic intermediate of brefeldin A from optically pure 2- and 3-oxy-4-pentenylmalonate derivatives are also described. 相似文献
65.
Diphenyl sulphoxide (DPSO) reacts with an equimolar amount of potassium (K) in tetrahydrofuran (THF) at ?78° to form a reddish-black solution, giving an electron spin resonance (ESR) signal only below ?70°. The signal is attributed to a very labile DPSO anion radical. The solution of DPSO-K (1/1) reaction products reacts further with another molecular amount of K at this temperature to give no ESR signal. The DPSO-K (1/1) reaction products initiates the polymerization of acrylonitrile (AN), but not the polymerizations of methyl methacrylate (MMA), styrene (St) or isoprene (IP). The active species of the solution initiating the polymerization of AN is assumed to be potassium benzene sulphenate from analyses of the solution and the infra-red spectrum of AN oligomers obtained using the complex. The DPSO-K (1/2) reaction products solution initiates the polymerization of MMA, St and IP as well as AN. The active species initiating the polymerization of MMA, St or IP is assumed to be phenylpotassium. 相似文献
66.
N. Momoshima N. Inoue Y. Takashima 《Journal of Radioanalytical and Nuclear Chemistry》1991,155(5):335-342
Loss of99Tc in seaweed during dry ashing has been investigated. Two kinds of brown seaweeds labeled with99Tc were ashed for 24 or 48 h at 400, 450 and 500 °C, showing no correlation between the loss of99Tc and species, temperature and time of ashing. The averaged recovery of99Tc was 91.0±4.0%, indicating that most of the99Tc in the seaweed was retained within the matrix of the ash which was obtained under general conditions of ashing. 相似文献
67.
68.
Yamada K Yagishita S Tanaka H Tohyama K Adachi K Kaizaki S Kumagai H Inoue K Kitaura R Chang HC Kitagawa S Kawata S 《Chemistry (Weinheim an der Bergstrasse, Germany)》2004,10(11):2647-2660
Novel metal-complex assemblies constructed from the flexible hinge-like ligand H(2)bhnq (H(2)bhnq=2,2'-bi(3-hydroxy-1,4-naphthoquinone)) have been synthesized. The X-ray crystal structures of these compounds reveal that four types of architectures are accessible by variation of the metal ions. In copper(II) compounds 1-3, the chelating bhnq(2-) ions bridge copper(II) centers to form one-dimensional zigzag chains. The chains of 1-3 are arranged by hydrogen-bonding interactions and stacking interactions to produce porous structures. Cobalt(II) and zinc(II) compounds 4 and 5 form one-dimensional helical chains. In 4 and 5, the crystal packing induces spontaneous resolution of the helical chains with chiral cavities formed perpendicular to the helices. Nickel(II) compounds 6 and 7 form cyclic tetramers. The fourth architecture, a dimer (compound 8), is obtained by the reaction of zinc(II) and bhnq(2-) in MeOH. In these compounds, changes of the dihedral angles and the metal-coordination mode of the bhnq(2-) ion induce the structural versatility. The assemblies of the zigzag chains of the copper(II) compounds exhibit reversible vapochromic behavior. UV/Vis, powder X-ray diffraction, EPR, and adsorption isotherm measurements indicate that this vapochromic behavior is based on the hinge-like flexibility of the bhnq(2-) ion. 相似文献
69.
Three new disubstituted benzo-15-crown-5 derivatives (3-5) have been synthesized from 4',5'-bis(bromomethyl)benzo-15-crown-5 (2) and the corresponding alkanols in the presence of Na(2)S(2), and their complexation thermodynamics with light lanthanoid(III) nitrates (La-Gd) have been studied in anhydrous acetonitrile at 25 degrees C. Plots of K(S) against the reciprocal ionic diameter of lanthanoid exhibited monotonically declining pattern for the parent benzo-15-crown-5 (1) and 3 but showed a characteristic peak at Ce(3+) for 4 and 5. It is interesting to note that the simple extension of the alkyl side chains in 4 and 5 can alter the cation selectivity profiles of 1 and 3. Possessing two 2-oxapropyl groups, 3 gave a comparable K(S) for La(3+) but a significantly decreased K(S) for Ce(3+) compared with the corresponding values for 1, thus exhibiting an exceptionally high La(3+)/Ce(3+) selectivity of 11. Thermodynamically, the complexation of lanthanoid perchlorates with 1 is absolutely entropy-driven in acetonitrile, while the complexation of lanthanoid nitrates with 3-5 is primarily driven by exothermic enthalpy changes with accompanying moderate entropic gain or small entropic loss. 相似文献
70.
A novel protocol for assembling polycyclic ethers was developed and successfully applied to the synthesis of the EFGH ring system of ciguatoxin CTX3C. A key transformation involves construction of an O,S-acetal through coupling of alpha-chlorosulfide and a secondary alcohol under mild conditions. The method is highly applicable to use with sensitive substrates and will enable the synthesis of various natural and artificial polycyclic ethers. [reaction: see text] 相似文献