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2.
Gerhard Buchbauer Waltraud Pernold Dorothea Rassl Brigitte Blach 《Monatshefte für Chemie / Chemical Monthly》1981,112(4):517-527
The synthesis of some new potentially, nitrogenefree spasmolytics is described. Formally the benzene nucleus in some mandelic acid esters, known by their mild spasmolytic activity, is substituted for the isocamphane bicyclus by a) SeO2 oxidation of 1-(3,3-Dimethyl-2-exo-norbornyl)-ethanone (5) to the corresponding ketoaldehyde6, b) oxidation of6 to the isocamphane analogous mandelic acid4 and c) esterification of derivatives of4 with isoamylalcohol and benzylalcohol. Attemps to dehydrate the methylester7 to camphenylideneacetic acid methylester (12) by various methods failed, probably because of the ring strain.
Teil der Diplomarbeit vonB. Blach, Universität Wien 1981. 相似文献
3.
A chiral supramolecular assembly encapsulates the two cationic ruthenium sandwich complexes [CpRu(eta(6)-C(6)H(6))](+) and [CpRu(p-cymene)](+). The host-guest complexes K(11)[CpRu(eta(6)-C(6)H(6)) subset Ga(4)L(6)] (2) and K(11)[CpRu(p-cymene) subset Ga(4)L(6)] (3) were characterized by one- and two-dimensional NMR techniques as well as by electrospray mass spectrometry. Encapsulation of the prochiral complex [CpRu(p-cymene)](+) by the chiral host renders enantiotopic protons diastereotopic as evidenced by (1)H NMR spectroscopy. 相似文献
4.
John K. Gallos Pygmalion S. Lianis Demetrios N. Nicolaides 《Journal of heterocyclic chemistry》1989,26(5):1415-1420
Reactions of furazano[3,4-b]quinoxalines 1 with phosphorus ylides 2 afford the transylidation product 3 and/or 4,9-dihydrofurazano[3,4-b]quinoxalines 4. Oxidation of 3 with phenyliodide bis-trifluoroacetate gave the fused furan derivative 13 in high yield. 相似文献
5.
Fiedler D Leung DH Bergman RG Raymond KN 《Journal of the American Chemical Society》2004,126(12):3674-3675
A supramolecular metal-ligand assembly encapsulates a variety of cationic half-sandwich ruthenium complexes. Due to the chirality of both host and guest, chiral recognition is observed with diastereomeric excesses up to 70%. The chiral cavity can be used to carry out a dynamic resolution of the rapidly equilibrating enantiomers of the chiral organometallic guest. 相似文献
6.
A new synthetic approach toward 2-C-methyl-d-erythritol 4-phosphate (MEP), a key intermediate in the mevalonate-independent biosynthetic pathway for isoprenoids, and deuterated analogues of its precursor, 2-C-methyl-d-erythritol acetonide, is described. This procedure uses 2-C-methyl-d-erythrose acetonide as starting material and delivers, through a mono-protection strategy, the target compounds in a short way and in high yield. 相似文献
7.
8.
Niko Kivel Dorothea Schumann Ines Günther-Leopold 《Analytical and bioanalytical chemistry》2013,405(9):2965-2972
In many scientific fields, the half-life of radionuclides plays an important role. The accurate knowledge of this parameter has direct impact on, e.g., age determination of archeological artifacts and of the elemental synthesis in the universe. In order to derive the half-life of a long-lived radionuclide, the activity and the absolute number of atoms have to be analyzed. Whereas conventional radiation measurement methods are typically applied for activity determinations, the latter can be determined with high accuracy by mass spectrometric techniques. Over the past years, the half-lives of several radionuclides have been specified by means of multiple-collector inductively coupled plasma mass spectrometry (MC-ICP-MS) complementary to the earlier reported values mainly derived by accelerator mass spectrometry. The present paper discusses all critical aspects (amount of material, radiochemical sample preparation, interference correction, isotope dilution mass spectrometry, calculation of measurement uncertainty) for a precise analysis of the number of atoms by MC-ICP-MS exemplified for the recently published half-life determination of $^{60}$ Fe (Rugel et al, Phys Rev Lett 103:072502, 2009). 相似文献
9.
H. D. Rozenfeld L. K. Gallos H. A. Makse 《The European Physical Journal B - Condensed Matter and Complex Systems》2010,75(3):305-310
We study the explosive character of the percolation transition in a
real-world network. We show that the emergence of a spanning cluster
in the Human Protein Homology Network (H-PHN) exhibits similar
features to an Achlioptas-type process and is markedly different from
regular random percolation. The underlying mechanism of this
transition can be described by slow-growing clusters that remain
isolated
until the later stages of the process, when the addition of a small number of
links leads to the rapid interconnection of these modules into a giant cluster.
Our results indicate that the evolutionary-based process that shapes
the topology of the H-PHN through
duplication-divergence events may occur in sudden steps, similarly to
what is seen in first-order phase transitions. 相似文献
10.