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11.
B. A. Arbuzov O. Éxsner A. P. Timosheva V. E. Kataev S. G. Vul'fson A. N. Vereshchagin 《Russian Chemical Bulletin》1976,25(6):1206-1212
1. | The dipole moments of the two kinds of C-O bonds in acetals and their analogs are not identical. |
2. | In formal molecules and the dimethylketal of acetone the C-O-C-O -C chains have gauche-gauche conformation, with the methyl groups lying on different sides of the O-C-O plane. |
3. | The dimethylketal of tetrachlorocyclopentadienone is represented by a mixture of trans-gauche and gauche-gauche conformers. |
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13.
A.?R.?MustafinaEmail author L.?S.?Kuznetsova A.?S.?Michailov V.?E.?Kataev A.?I.?Konovalov W.?D.?Habicher 《Journal of solution chemistry》2004,33(10):1257-1276
The complexation of a macrocycle containing thiopyrimidine and uracil moieties (M) with amino acids and some dicarboxylic acids was studied by pH-metric, UV-VIS, 1H NMR spectroscopy methods in chloroform, methanol, aqueous 1,4-dioxane, and biphasic water–chloroform media. The complexation of M with acids is too weak to solubilize them from the solid state into chloroform solutions containing M. The 1H NMR spectra and pH-metric data of aqueous 1,4-dioxane (80 vol.%) reveal the pH-dependent 1:1 binding between M and the acids studied. The protonation of M is not a prerequisite for binding of fumaric, succinic, o-phtalic acids and the series of amino acids, whereas binding of maleic acid requires the protonation of both thiopyrimidine moieties of M. Therefore,M·(H+)2 exhibits strong selectivity towards maleic acid in aqueous 1,4-dioxane and in biphasic water–chloroform media. 相似文献
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R. R. Sharipova O. A. Lodochnikova I. Yu. Strobykina R. Z. Musin V. M. Babaev V. I. Morozov S. N. Pod“yachev R. V. Chestnova V. E. Kataev 《Russian Chemical Bulletin》2013,62(1):175-182
New nitrogen-containing derivatives of the diterpenoid isosteviol (16-oxo-ent-beyeran-19-oic acid) containing oxo, hydroxyimine, and thiosemicarbazone groups were synthesized. Isosteviol 15-oxo-16-thiosemicarbazone forms a 1: 1 complex with CuII and inhibits the growth of Mycobacterium tuberculosis (H37RV, in vitro) at the minimum inhibitory concentration of 20 μg mL?1. 相似文献
16.
We obtain analytical five-loop results for the renormalization group ??-function of Quantum Electrodynamics with the single lepton in different renormalization schemes. The theoretical consequences of the results obtained are discussed. 相似文献
17.
Strobykina I. Yu. Andreeva O. V. Garifullin B. F. Sharipova R. R. Kataev V. E. 《Russian Journal of General Chemistry》2017,87(3):579-582
Russian Journal of General Chemistry - 3β-O-Acetyl-28-O-succinyl-(2,3,4-tri-O-acetyl-5-methoxycarbonyl-β-D-glucopyranosyl)dihydrobetulin was synthesized. 相似文献
18.
Conditions of the simultaneous isolation of various types of zolpidem metabolites from samples of real urine by solid-phase extraction have been optimized. Various derivatives of zolpidem hydroxy- and carboxy-metabolites were obtained; their mass-spectral and gas-chromatographic characteristics have been studied. The results ensure the reliable identification of zolpidem metabolites by gas chromatography-mass spectrometry for chemical toxicological and forensic investigations. 相似文献
19.
New thietanyl-substituted derivatives of pyrimidine-2,4(1H,3H)-dione and imidazole were synthesized. The alkylation of 6-methylpyrimidine-2,4(1H,3H)-diones with 2-chloromethylthiirane in water involved the N1 atom of the pyrimidine ring and afforded 6-methyl-1-(thietan-3-yl)-pyrimidine-2,4(1H,3H)-diones. Under analogous conditions 6-aminopyrimidine-2,4(1H,3H)-dione gave rise to 6-(thietan-3-ylamino)pyrimidine-2,4(1H,3H)-dione. Unsymmetrically substituted 2-methyl-4(5)-nitro- and 5(4)-bromo-2-methyl-4(5)-nitro-1H-imidazoles reacted with 2-chloromethylthiirane to produce mixtures of isomeric 2-methyl-4(5)-nitro-1-(thietan-3-yl)-1H-imidazoles and 5(4)-bromo-2-methyl-4(5)-nitro-1-(thietan-3-yl)-1H-imidazoles. 相似文献
20.
Prof. Evgeny A. Kataev Dr. Grigory V. Kolesnikov Rene Arnold Herman V. Lavrov Prof. Victor N. Khrustalev 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(11):3710-3714
Inorganic anions were used as templates in the reaction between a diamine and an activated diacid to form macrocyclic amides. The reaction conditions were found to perform the macrocyclization sufficiently slow to observe a template effect. A number of analytical methods were used to clarify the reaction mechanisms and to show that the structure of the intermediate plays a decisive role in determining the product distribution. For the macrocyclization under kinetic control, it was shown that the amount of a template, the conformational rigidity of building blocks, and the anion affinities of reaction components and intermediates are important parameters that one should take into consideration to achieve high yields. 相似文献