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排序方式: 共有126条查询结果,搜索用时 15 毫秒
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32.
Dr. Xiao Shen Constanze N. Neumann Claudia Kleinlein Nathaniel W. Goldberg Prof. Dr. Tobias Ritter 《Angewandte Chemie (International ed. in English)》2015,54(19):5662-5665
An alkyl aryl ether bond formation reaction between phenols and primary and secondary alcohols with PhenoFluor has been developed. The reaction features a broad substrate scope and tolerates many functional groups, and substrates that are challenging for more conventional ether bond forming processes may be coupled. A preliminary mechanistic study indicates reactivity distinct from conventional ether bond formation. 相似文献
33.
We study once‐reinforced random walk on . For this model, we derive limit results on all moments of its range using Tauberian theory. 相似文献
34.
Peter Thumbs Timm T. Ensfelder Markus Hillmeier Mirko Wagner Matthias Heiss Constanze Scheel Alexander Schn Markus Müller Stylianos Michalakis Stefanie Kellner Thomas Carell 《Angewandte Chemie (International ed. in English)》2020,59(30):12352-12356
Queuosine (Q) is a hypermodified RNA nucleoside that is found in tRNAHis, tRNAAsn, tRNATyr, and tRNAAsp. It is located at the wobble position of the tRNA anticodon loop, where it can interact with U as well as C bases located at the respective position of the corresponding mRNA codons. In tRNATyr and tRNAAsp of higher eukaryotes, including humans, the Q base is for yet unknown reasons further modified by the addition of a galactose and a mannose sugar, respectively. The reason for this additional modification, and how the sugar modification is orchestrated with Q formation and insertion, is unknown. Here, we report a total synthesis of the hypermodified nucleoside galactosyl‐queuosine (galQ). The availability of the compound enabled us to study the absolute levels of the Q‐family nucleosides in six different organs of newborn and adult mice, and also in human cytosolic tRNA. Our synthesis now paves the way to a more detailed analysis of the biological function of the Q‐nucleoside family. 相似文献
35.
Eugen Wuckert Sabine Laschat Angelika Baro Constanze H gele Frank Giesselmann Heinrich Luftmann 《Liquid crystals》2006,33(1):103-107
We report the synthesis and liquid crystalline properties of novel ester-substituted tetraphenylenes obtained from octamethoxytetraphenylene by demethylation and esterification. The target compounds display focal-conic textures typical for columnar mesophases, which are either rectangular or hexagonal columnar in nature, depending on the alkyl chain length. 相似文献
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An unresolved structural issue for [FeFe]-hydrogenases is the nature of the dithiol-bridging ligand in the diiron subcluster of the active site. The two most probable candidates are 1,3-dithiopropane (propane dithiol, PDT) and di-(thiomethyl)-amine (DTN). In the latter case, the dithiol-bridging ligand is assumed to play a major role in the reaction cycle. We report density-functional theory studies of the differing roles of these dithiol-bridging ligands in the infrared spectra of synthetic models and of computational representations of the diiron cluster of the active site. Our analysis shows distinct spectral features associated with the dithiol-bridging NH mode for compounds having a DTN bridge, which, however, would have been obscured by the H2O vibrations in existing measurements. However, if indeed nitrogen is present in the dithiol-bridging ligand, a combination of selective deuteration and chemical inactivation with CO would create a unique signature in an accessible region of the infrared spectrum, whose position and intensity are predicted. 相似文献
39.
Strojek W Fehse CM Eckert H Ewald B Kniep R 《Solid state nuclear magnetic resonance》2007,32(3):89-98
A comprehensive solid-state NMR investigation on crystalline Na(5)B(2)P(3)O(13) is presented. Triple-quantum magic angle spinning (TQMAS) and rotational echo double resonance (REDOR) studies are used for accurate determinations of the (11)B, (23)Na and (31)P interaction parameters. Based on these results and complementary quantum mechanical calculations, plausible site assignments can be derived. Generally, the results show that detailed, quantitative information about structures in borophosphate compounds can be obtained by investigating both the local site environments characterized by chemical shift and quadrupolar interaction parameters and the correlated dipolar interactions to atoms in the second coordination sphere. 相似文献
40.
Kanawati B von Saint Paul V Herrmann C Schäffner AR Schmitt-Kopplin P 《Rapid communications in mass spectrometry : RCM》2011,25(6):806-814
L-Ascorbic acid and two distinct anomers, namely the α-D-glucopyranosyl and β-D-glucopyranosyl-(1→2)-L-ascorbic acid (stereoisomers), were studied within the scope of collision-induced dissociation (CID) experiments, performed by linear ion acceleration and collision with argon atoms inside a hexapole quadrupole hexapole ion beam guide, which is coupled to an ion cyclotron resonance (ICR) cell with a 12 Tesla magnet for high-resolution measurements. Loss of C(2)H(4)O(2) neutral from the [M-H](-) anion of L-ascorbic acid was observed. Density functional theory (DFT) calculations on the 6-311+G(2d,p)//6-31+G(d) level of theory reveal a new concerted mechanism for an intramolecular gas-phase rearrangement, through which the observed ejected neutral C(2)H(4)O(2) can take place. A similar rearrangement also occurs in the case of α- and β-D-glucopyranosyl-(1→2)-L-ascorbic acid. For the α isomer, only homolytic glycoside fragmentation was observed. For the β isomer, both homolytic and heterolytic glycoside cleavages were possible. The mechanisms behind all observed fragmentation pathways were fully understood by the implementation of accurate DFT calculations. Stereoisomeric differentiation between α and β isomers of the L-ascorbic acid-2-O-glucoside could be revealed by tandem mass spectrometry (MS/MS) experiments and were explained theoretically. 相似文献