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91.
Shindo M Sato Y Koretsune R Yoshikawa T Matsumoto K Itoh K Shishido K 《Chemical & pharmaceutical bulletin》2003,51(4):477-478
Aliphatic alpha,alpha-dibromo esters, precursors of ynolates, were synthesized via bromination of lithium alpha-bromo ester enolates with 1,2-dibromotetrafluoroethane in good yields. alpha-Trimethylsilyl-alpha,alpha-dibromo esters were synthesized via radical bromination. 相似文献
92.
Maezaki N Yagi S Yoshigami R Maeda J Suzuki T Ohsawa S Tsukamoto K Tanaka T 《The Journal of organic chemistry》2003,68(14):5550-5558
Unprecedented Pd-catalyzed sulfinylzincation with 1-alkynyl sulfoxide as a sulfinyl source was developed. Bis-sulfinyl alkenes were formed in good yields on treatment of 1-alkynyl sulfoxides with Et(2)Zn in the presence of a Pd-catalyst, wherein zinc sulfenate (or sulfinylzinc) species would be generated in situ to undergo highly syn-selective conjugate addition to the 1-alkynyl sulfoxides. By using 3,3-dimethyl-1-butynyl sulfoxides, formation of the bis-sulfinyl alkenes was completely suppressed and the sulfinylzincation of activated alkynes was accomplished. The reaction tolerates various functionalities, and was promoted considerably by the neighboring group participation of the heteroatom at the delta-position in the alkynoates. Stereodivergent synthesis of two diastereomeric vinylic sulfoxides and reaction of the resulting vinylzinc species with electrophiles were also described. 相似文献
93.
[reaction: see text] A new synthetic method of chiral beta,beta-disubstituted vinylic sulfoxides bearing various functionalities has been developed by employing Cu-catalyzed conjugate addition of an organozinc reagent to chiral 1-alkynyl sulfoxide. Since the reaction proceeds with very high syn-selectivity, both geometric beta,beta-disubstituted vinylic sulfoxides were stereoselectively synthesized by changing the combination of 1-alkynyl sulfoxide and the organozinc reagent. 相似文献
94.
A highly beta-selective C-allylation of 2,3-O-(3-pentylidene)-D-ribofuranosyl fluoride is described. This strategy will provide a new concept for synthesizing beta-C-ribosides by controlling the effect of steric hindrance in the transition state. 相似文献
95.
An efficient enantioselective synthesis of sn-2-aminooxy (AO) analogues of lysophosphatidic acid (LPA) that possess palmitoyl and oleoyl acyl chains is presented. Both sn-2-AO LPA analogues are agonists for the LPA1, LPA2, and LPA4 G-protein-coupled receptors, but antagonists for the LPA3 receptor and inhibitors of autotaxin (ATX). Moreover, both analogues stimulate migration of intestinal epithelial cells in a scratch wound assay. 相似文献
96.
Kitano K Kuwamura N Tanaka R Santo R Nishioka T Ichimura A Kinoshita I 《Chemical communications (Cambridge, England)》2008,(11):1314-1316
Tris(2-pyridylthio)methane (tptmH) reacts with ZnCl(2) producing the Zn-C containing complex of [ZnCl(tptm)], whose cyclic voltammogram shows an irreversible oxidation peak at 0.2 V vs. E(0')(Fc(+/0)). DFT calculations suggested that 1e(-) oxidation should occur at the tptm ligand resulting in the cleavage of the Zn-C bond, leading to decomposition of the complex. 相似文献
97.
Well-defined polymer brushes and block copolymer brushes consisting of 2-methacryloyloxyethyl phosphorylcholine (MPC) and glycidyl methacrylate (GMA) were prepared by surface-initiated atom transfer radical polymerization (ATRP). The polymer brushes were used for the immobilization of antibody fragments in a defined orientation. Pyridyl disulfide moieties were introduced to the polymer brushes via a reaction of epoxy groups in GMA units. Fab’ fragments were then immobilized onto these surfaces via a thiol-disulfide interchange reaction and the reactivity of antibodies with antigens was investigated. Antigen/antibody binding on the polymer brushes was more preferable than that on epoxysilane films as a control surface. Furthermore, the activity of the antibodies immobilized on the block copolymer brushes having biocompatible PMPC was greater than that on other surfaces that did not have PMPC in their structures. 相似文献
98.
Fluid permeability of polydisperse particulate bed with finite thickness has been examined. On the assumption of creeping flow, the permeability of monodisperse particles with arbitrary arrangement is calculated by means of Stokesian dynamics approach in which the interaction between individual particles and interstitial fluid is described by multipole expansion of the Oseen tensor. We have extended such calculation method to polydisperse particulate systems which have not so dense structures (up to particle volume fraction ${\phi \sim}$ 0.2). The particles are located infinitely in space and their interaction has been taken into account by Ewald summation technique. For the spatial distribution of polydisperse particles, we consider locally stratified particulate beds and define stratification degree as a parameter which apparently and mathematically represents the thickness of the mixing region of different-sized particles. The permeability profiles in the particulate beds with different stratification degree show the dependence of local permeability on the spatial and size distribution of particles. Consequently, the calculation results indicate that the permeability of non-uniform polydisperse particulate bed can be predicted by integrating the local permeation resistance which is determined by the local specific surface area. 相似文献
99.
Journal of Visualization - The effect of fiber tortuosity on fluid permeability in fibrous beds has been investigated. A particle model is employed in which a fiber is replaced by spherical... 相似文献
100.