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881.
882.
1,3-Dipolar cycloaddition of 2-arylidene-6,7-dihydro-5H-thiazolo[3,2-a]pyrimidine-3(5H)-ones to diphenylnitrilimine (generated in situ by triethylamine dehydrohalogenation of the N′-phenylbenzohydrazonoyl chloride) proceeded regio- and site-selectively affording a mixture of two unexpected isomer products at reflux temperature. The cycloaddition/ring-opening/rearrangement/substitution, mechanism of the reaction was also discussed. 相似文献
883.
R. Anjibabu Samaresh Sau B. Jagan Mohan Reddy Rajkumar Banerjee B.V. Subba Reddy 《Tetrahedron letters》2013
A variety of aldehydes undergo a smooth coupling with (4-methylcyclohex-3-en-1-yl)methanol in the presence of 2 mol % of phosphomolybdic acid in dichloromethane to afford 3-oxabicyclo[3.3.1]non-7-ene in good yields through 3,5-oxonium-ene cyclization under mild conditions. The use of inexpensive, nontoxic, and readily available heteropoly acid catalyst makes this method simple, convenient, and environmental-friendly. 相似文献
884.
The domino reactions of (E)-2-(aryl)-2,3-dihydro-1H-inden-1-ones and 1,4-dithiane-2,5-diol in the presence of triethylamine in water stereoselectively afforded a library of 2′-(aryl)-4′-hydroxy-4′,5′-dihydro-2′H-spiro[indene-2,3′-thiophen]-1(3H)-ones. This transformation presumably proceeds via the generation of 2-mercaptoacetaldehyde from 1,4-dithiane-2,5-diol followed by Michael addition–intramolecular aldol sequence with C–C and C–S bond formations and creation of three contiguous stereocenters in a one-pot operation. 相似文献
885.
Elisabeth Siebert Marius Horch Yvonne Rippers Johannes Fritsch Stefan Frielingsdorf Oliver Lenz Francisco VelazquezEscobar Friedrich Siebert Lars Paasche Uwe Kuhlmann Friedhelm Lendzian Maria‐Andrea Mroginski Ingo Zebger Peter Hildebrandt 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2013,125(19):5267-5270
886.
The effect of cationic micelles of cetyltrimethyl ammonium bromide (CTAB) on the observed pseudo-first-order rate constant for the interaction of nickel dipeptide complex [Ni(II)-Gly-Gly]+ with ninhydrin has been studied spectrophotometrically. At constant temperature and pH, increase in the [CTAB] from 0.0 to 60.0 × 10?3 mol dm?3 caused nearly three-fold increase of the rate constant. The micellar catalysis is explained in terms of the pseudophase model. From the observed kinetic data, binding constants of micelle–[Ni(II)-Gly-Gly]+ (K S), and micelle–ninhydrin (K N) are evaluated, respectively, to be 5.3 mol?1 dm3 and 84.0 mol?1 dm3. The role of added inorganic (NaCl, NaBr, Na2SO4) and organic salts (NaBenz, NaSal) on the reaction rate has also been examined. 相似文献
887.
888.
LUO Ya-Nan XU Xian-Zhua YU Xiao-Yang ZHU Guang-Shan QU Xiao-Shu ZHANG Xiao YU Li-Ying 《结构化学》2013,(11):1667-1672
A new coordination polymer, {[CdL(en)]'DMF}n (1, H2L = 4-[(8-hydroxy-5- quinolinyl)azo]-benzenesulfonic acid, en = ethylenediamine, DMF = N,N-dimethylformamide), has been solvothermally synthesized and structurally characterized by single-crystal X-ray diffrac- tion, infrared (IR) spectra, elemental analysis, powder X-ray diffractions (PXRD) and thermo- gravimetric analysis (TGA). Compound 1 crystallizes in monoclinic, space group P2Jc with a = 14.6525(9), b = 13.3917(9), c = 11.8838(8) A, β = 101.2290(10)°, V = 2287.2(3) A3, Z = 4, C20H24CdN6OsS, Mr = 572.91, Dc. = 1.664 mg-mm-3, F(000) = 1160, p = 1.091 mm-1, R = 0.0232 and wR = 0.0587 for 3597 observed reflections (I 〉 2σ(I)). Compound 1 exhibits a one-dimensional (1D) double-chain structure which is further connected through hydrogen bonding and π-π interactions into a three-dimensional (3D) supramolecular network. In addition, it exhibits blue fluorescence at room temperature in the solid state. 相似文献
889.
Indolocarbazole derivatives have been reported to be promising organic semicon- ductor candidates and electroluminescent (EL) materials. One novel indolocarbazole derivative, 2,8-acetyl-5,11-dihexyl-6,12-(di-p-tolyl)-5,11-indolo[3,2-b]carbazole (YK4), has been synthesized, and its crystal structure has also been carefully studied. YK4 is triclinic, space groups Pi with a = 9.409(5), b = 13.974(5), c = 15.488(5) A, α = 90.281(5), β = 105.456(5), Z= 93.728(5)°, M,. = 688.94, V= 1958.1(14) A3, Z = 2, Dc.= 1.168 g/cm-3,μ = 0.070 mm-1, F(000) = 740, Rint = 0.0475, R (I〉 20(/)) = 0.1146, wR (I〉 20(/)) = 0.2186, R(all data) = 0.2192 and wR (all data) = 0.2701. Like other indolo[3, 2-b]carbazole derivatives which were introduced in the 5- and 11-positions, the intermolecular short contacts are localized between the pendant groups and acetyl groups of the neighboring indolocarbazole molecules. The molecule of YK4 possesses poor face-to-face π-π stacking between two adjacent molecules in the crystal. The calculated bond lengths and bond angles of YK4 also proved the result of crystallography. 相似文献
890.
Janaína Versiani dos Anjos Rajendra M. Srivastava Silene Carneiro do Nascimento Sebastião J. de Melo 《Journal of carbohydrate chemistry》2013,32(4):258-277
A copper‐catalyzed reaction of propargyl 4,6‐di‐O‐acetyl‐2,3‐dideoxy‐α‐D‐erythro‐hex‐2‐enopyranoside with 3‐(4‐azidophenyl)‐1,2,4‐oxadiazoles gave the corresponding hexenopyranosides bearing an 1,2,4‐oxadiazole subunit in the aglyconic part of the molecule. The same reaction between ethyl 4‐azido‐2,3,4‐trideoxy‐α‐D‐erythro‐hex‐2‐enopyranoside and acetylenic 1,2,4‐oxadiazoles afforded the corresponding hexenopyranosides carrying a triazole and a 1,2,4‐oxadiazole ring at C‐4 of the carbohydrate. Combination of the two sequences gave hexenopyranosides displaying two 1,2,4‐oxadiazole subunits, each one being embedded in the C‐1 and C‐4 frameworks, of the carbohydrate moiety. A simple dihydroxylation reaction of these unsaturated carbohydrates yielded a series of mannopyranosides bearing one or two 1,2,4‐oxadiazole subunits at C‐1 or C‐4. These new compounds were evaluated for their cytotoxic activities against two cell strains: NCI‐H292 (lung carcinoma) and Hep‐2 (larynx carcinoma), some of them presenting impressive cell growth inhibitions. 相似文献