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11.
A concise total synthesis of PDE-I and -II featuring copper-mediated double aryl amination with the combination of CuI, CsOAc, and Cs2CO3 is described. The highly substituted pyrroloindole skeleton was constructed by a one-pot five-step sequence including double aryl amination, β-elimination, deprotection of a Cbz group, and unexpected formation of an indole via removal of an Ns group followed by rearomatization. The undesired elimination of the protecting group (Ns group) was hampered by using the Boc group as a protecting group in the second-generation synthesis, which excluded the reduction of the indole required in the first-generation synthesis.  相似文献   
12.
Cascade reactions of nitroallylic acetates with methanesulfonyl 2-aminoethanones affords either the 3-pyrrolines or the pyrroles in one pot depending on reaction solvents and temperature. A possible mechanism for the entire sequence is proposed.  相似文献   
13.
Controlling reaction selectivity is an eternal pursuit for chemists working in chemical synthesis. As part of this endeavor, our group has been exploring the possibility of constructing different natural product skeletons from the same simple starting materials by using different catalytic systems. In our previous work, an isoflavanone skeleton was obtained from the annulation of a salicylaldehyde and an alkyne when a gold catalyst was employed. In this paper, it is shown that a coumarin skeleton can be efficiently obtained through an annulation reaction with the same starting materials, that is, terminal alkynes and salicylaldehydes, by simply switching to a rhodium catalyst. A plausible reaction mechanism is proposed for this new annulation based on isotopic substitution experiments.  相似文献   
14.
The first highly asymmetric catalytic synthesis of densely functionalized dihydrobenzofurans is reported, which starts from ortho-hydroxy-containing para-quinone methides. The reaction relies on an unprecedented formal [4+1]-annulation of these quinone methides with allenoates in the presence of a commercially available chiral phosphine catalyst. The chiral dihydrobenzofurans were obtained as single diastereomers in yields up to 90 % and with enantiomeric ratios up to 95:5.  相似文献   
15.
A novel, rational‐designed approach to access various heteroaryl‐substituted alkyl thioethers was developed via docking‐migration cascade process. By utilizing three components involving alkene, dual‐function reagent, and thioetherificating reagent, radical heteroarylalkylation of alkenes followed by thiolation of the alkyl radical intermediates proceeded smoothly, manifesting well compatibility of substrates and cascade transformations. Furthermore, this protocol also features mild conditions, broad substrate scope, and wide product diversity.  相似文献   
16.
A cobalt(II)-catalyzed [4+2] annulation of picolinamides with alkynes via C−H bond activation has been developed. The operationally simple annulation reaction allows for the synthesis of acyl-substituted 1H-benzoquinoline bearing multiple aromatic rings (up to 96 % yield) without co-oxidant or other oxidation factors under mild conditions. Several control experiments were carried out. This practical [4+2] annulation provides an efficient route to access highly functionalized compounds.  相似文献   
17.
Reported herein is an intramolecular 1,3-dipolar cycloaddition strategy for rapid entry into benzopyranopyrazoles (BPP) on water medium as “open flask chemistry” approach. The in situ generation of diazo functionality in two-step sequence from the appropriate alkylated salicylaldehydes undergoes smooth [3?+?2]-cycloaddition with unactivated alkynes/alkenes furnishing benzopyranopyrazoles in good yield. This methodology was also extended for the synthesis of pyrazole incorporated macrocycles. This cascade protocol involving water medium provides an atom-economical and environment friendly approach.  相似文献   
18.
The optimal weighting scheme and the role of coupling strength against load failures on symmetrically and asymmetrically coupled interdependent networks were investigated. The degree-based weighting scheme was extended to interdependent networks, with the flow dynamics dominated by global redistribution based on weighted betweenness centrality. Through contingency analysis of one-node removal, we demonstrated that there still exists an optimal weighting parameter on interdependent networks, but it might shift as compared to the case in isolated networks because of the break of symmetry. And it will be easier for the symmetrically and asymmetrically coupled interdependent networks to achieve robustness and better cost configuration against the one-node-removal-induced cascade of load failures when coupling strength was weaker. Our findings might have great generality for characterizing load-failure-induced cascading dynamics in real-world degree-based weighted interdependent networks.  相似文献   
19.
In this paper, we present a novel method to detect license plates in video sequences automatically. The framework mainly integrates the cascade detectors method and the Tracking Learning Detection (TLD) algorithm. The cascade detectors are used to detect license plates, and the TLD algorithm is adopted to track the license plate regions. The license plates in the first frame image are detected by the cascade detectors to build the original tracking list, the tracking results and the detection results in following frames will be compared, and the newly appearing license plate information will be added to the tracking list. Meanwhile, the tracking results existing in the current tracking list would be replaced by the corresponding detection results with higher degree of confidence. We demonstrate the effectiveness of our algorithm for license plate detection task on a road intersection dataset, and the experimental evaluation shows the detection performance has been greatly improved by synthetically using the detection and tracking strategy.  相似文献   
20.
Palladium-catalyzed [4+2] oxidative annulation of coumarin-benzimidazoles with olefins for the synthesis of polycyclic aromatic hydrocarbons have been achieved. This synthetic protocol gives access to a wide range of structurally distinct imidazo[1,2-a]chromeno[3,4-c]pyridines in moderate to good yield with wide functional group tolerance. Further, photophysical properties of annulated scaffolds have been examined, which discloses their interesting solvatochromic emission behaviors.  相似文献   
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