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141.
Takumi Kongo 《International Journal of Game Theory》2010,39(4):669-675
The study characterizes the position value and the Myerson value for communication situations. Each of these two values is represented by the Shapley value of a modified game obtained from the original communication situation. The difference between the two values comes from the existence of a coalition structure in the modified game. 相似文献
142.
Three new amino acid derivatives (1-3) and three known ones (4-6) were isolated from the mushroom Pleurocybella porrigens. The structures of 1-6 were determined by the interpretation of spectroscopic data. Compounds 1, 3, 4, and 5 were toxic to mouse cerebrum glial cells. 相似文献
143.
Here, we report a unique mesoporous ionic solid (I) generated from a cationic AuI6AgI3CuII3 dodecanuclear complex with d-penicillamine depending on the homochirality and crystallization conditions. I crystallizes in the cubic space group of F4132 with an extremely large cell volume of 2 171 340 Å3, containing 272 AuI6AgI3CuII3 complex cations in the unit cell. In I, the complex cations are connected to each other through CH⋯π interactions in a zeotype framework, the topology of which is the same as that of the metal–organic framework in MIL-101, with similar but much larger two types of polyhedral pores with internal diameters of 38.2 Å and 49.7 Å, which are occupied by counter-anions and water molecules. Due to the cationic nature of the framework, I undergoes quick, specific exchanges of counter-anions while retaining its single crystallinity. This study realized the creation of a non-covalent mesoporous framework from a single complex salt, providing a conceptual advance in solid chemistry and material science.A non-MOF ionic solid having two types of polyhedral mesopores in a very large crystal lattice is generated from a cationic AuI6AgI3CuII3 complex with d-penicillamine, showing specific exchanges of counter-anions retaining its single crystallinity. 相似文献
144.
The reaction of dimethyl(methylthio)sulfonium trifluoromethanesulfonate (DMTST) with o-allylphenol gave 2-methylthiomethyl-2,3-dihydrobenzofuran in 97% yield. The reaction of DMTST with N-tosyl-o-isopropenylanilide followed by the addition of aq sodium carbonate afforded N-tosyl-3-methylindole in 88% yield, whereas N-tosyl-o-vinylanilide afforded N-tosylindoline in 85% yield. 相似文献
145.
Seunghee Jung Yuki TsukudaRie Kawashima Takumi IshikiAyaka Matsumoto Aya NakaniwaMiho Takagi Takuya NoguchiNobuyuki Imai 《Tetrahedron letters》2013
Acetaminophen analogues containing α-amino acid and fatty acids were easily synthesized in 77–99% yields from the corresponding mixed carbonic carboxylic anhydrides of α-amino acid and fatty acids using aniline derivatives in aqueous MeCN. 相似文献
146.
[reaction: see text] The enantioselective conjugate addition reaction of Et(2)Zn to Meldrum's acid derived acceptors, mediated by a catalyst formed from Cu(O(2)CCF(3))(2) and a phosphoramidite ligand, is reported. Adducts are obtained in useful yields and up to 94% ee. 相似文献
147.
Tsutomu Kumagai Takumi Nittono Noriyuki Tanaka Toshio Mukai 《Tetrahedron letters》1985,26(49):6093-6096
Upon irradiation, 2-dicyanomethylenebenzonorbornene f was converted into 1-dicyanomethylenebenzobicyclo[3.1.1]heptene . The reaction pathway is discussed with reference to the photoreaction of parent hydrocarbon. 相似文献
148.
Tsutsui H Abe T Nakamura S Anada M Hashimoto S 《Chemical & pharmaceutical bulletin》2005,53(10):1366-1368
An efficient and reliable procedure for the preparation of dirhodium(II) tetrakis[N-phthaloyl-(S)-tert-leucinate], Rh2(S-PTTL)(4), a universally effective catalyst for a range of enantioselective carbene transformations, is described. The N-phthaloylation of (S)-tert-leucine by the method of Bose with essentially no racemization is a key to this process. 相似文献
149.
球壳粒子悬浮系模型化研究——内部相参数对介电谱影响的数值模拟 总被引:2,自引:0,他引:2
在Hanai理论基础上对球壳粒子悬浮系的介电模型进行了模拟研究,通过用C++的复数类对理论公式的程序化,建立了介电谱的介电参数与体系内部相参数的关系.所得的解析解可方便地模拟介电弛豫谱依不同相参数的变化曲线,计算并分析了内部参数对介电谱的模式以及介电参数的影响因素. 相似文献
150.
Koizumi T Harada K Asahara H Mochizuki E Kokubo K Oshima T 《The Journal of organic chemistry》2005,70(21):8364-8371
Bicyclic 3aH-cyclopentene[8]annulene-1,4-(5H,9aH)-diones underwent three types of acid-induced transannular reactions, Michael cyclization, [3 + 2] cycloaddition, and Friedel-Crafts ipso-alkylation, depending on the cyclopentenone ring substituent (Me or Ph) and the position of [8]annulenone substituent as well as the nature of acids (BF3, MeSO3H, CF3SO3H). The Me-substituent permitted the Michael reaction for all acids used to give tricyclic diones by the activation of cyclopentenone carbonyl group. However, the Ph-substituent inhibited the Michael reaction for BF3 and MeSO3H but allowed the [3 + 2] cycloaddition and Friedel-Crafts reaction for CF3SO3H depending on the position of annulenone substituent. These CF3SO3H reactions exhibited the following novel rearrangements, affording 2-naphthalenone and 7-acenaphthylene derivatives, respectively. The factors that control the reaction mode of these transannular cyclizations were discussed in view of the constraint twist-boat conformation of [8]annulenone ring as well as the ring substituent effects on the intramolecular cyclization. In addition, these [8]annulenone rings were found to easily undergo the intramolecular [2 + 2] photocyclization to provide the tetracyclic cage compounds which exhibited the facile cycloreversion under the influence of acid. 相似文献