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1.
Using the Chern classes defined by Grothendieck, we map aK-theoretic invariant of invertible symmetric matrices defined by Giffen to the Clifford invariant.According to Herrmann Graßman'sWörterbuch zum Rig-veda, Ketu may not be connected with K2 but es bezeichnet das, was sich sichtbar oder kenntlich macht ... 相似文献
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The chemoselective reaction of hydrazine on the ketone rather than the ester in a gem diester system with a γ‐keto group by hydrazinium sulfate and a tandem deesterification of one of the esters in this system by N,N‐dimethylformamide are reported. 相似文献
4.
Chilakapati Venkata Vishnu Vardhan Sajal Ghosh Subramaniam Nagaraj Raghavachary Sridharan Thiagarajan Gnanasekaran 《Journal of Thermal Analysis and Calorimetry》2013,112(1):127-131
A study of binary, CaBr2–CaHBr system was carried out by differential thermal analysis (DTA), covering the composition range from 100 % CaBr2 to 100 % CaHBr between room temperature and 800 °C. From DTA results, the contour of solidus and liquidus temperatures with composition is plotted and the phase diagram of CaBr2–CaHBr system is constructed. The system shows an eutectic reaction at 576 °C and the eutectic composition is 79.6 mol% CaBr2. Co-existing phases in different phase fields are characterized by X-ray diffraction analysis. 相似文献
5.
S. Nagaraj C. V. Vishnuvardhan Sajal Ghosh R. Sridharan 《Journal of Thermal Analysis and Calorimetry》2014,115(2):1835-1839
The phase diagram of binary LiBr–CaBr2 system was investigated using differential thermal analysis (DTA) between room temperature and 800 °C. From the DTA results obtained over the entire range of composition from pure LiBr to pure CaBr2 in steps of ~5 mol%, the phase diagram was constructed and is reported here. The results indicated the possible existence of a compound at 50 mol% LiBr, namely, LiCaBr3. The compound undergoes peritectic decomposition at 552 °C. The system shows a eutectic reaction at 532 °C between this compound and LiBr phase, and the eutectic composition is close to 80 mol% LiBr. The compound LiCaBr3 decomposes into CaBr2 and LiBr phases below 272 °C. Co-existing phases in different phase fields are characterized by X-ray diffraction analysis. 相似文献
6.
Stephen Brown Ronald Grigg Joanne Hinsley Stewart Korn Visuvanathar Sridharan Michael D. Uttley 《Tetrahedron》2001,57(52):809-10355
A wide variety of aryl/heteroaryl iodides undergo an intermolecular Heck reaction with alkylallenes to furnish 1,3-dienes. These subsequently react in situ with various dienophiles to give Diels–Alder adducts. The chemistry has been extended to incorporate cyclisation-anion capture methodology and the stereochemistry of the products has been determined. 相似文献
7.
Sadaiyan Ramadass Jayapradha Vellaisamy Sridharan Shanmugam Muthusubramanian Kurt Polborn 《Journal of heterocyclic chemistry》2007,44(5):1105-1108
A new set of 2,3,4,5‐tetrasubstituted isoxazolidines with an α,β‐unsaturated carbonyl function at position 4 has been synthesized. The multicomponent approach and microwave irradiation protocol have also been investigated for the above synthesis. 相似文献
8.
Sridharan RajagopalMichael E Brooks Thach-Mien NguyenMichael Novak 《Tetrahedron》2003,59(40):8003-8010
We report the synthesis of N-acetoxy-N-(1-methyl-5H-pyrido[4,5-b]indol-3-yl)acetamide, 7, its N-pivaloyloxy analogue, 9, and improved synthesis of indole-2-acetonitrile, 3 (70% in five steps from indole-2-carboxylic acid), the carcinogenic amine Trp-P-2, 4 (40% from 3), and the nitro compound, 5 (40% from 4 by oxidation with H2O2 using Mo(CO)6 catalyst). In aqueous solution at neutral pH, 7 primarily undergoes C-O bond cleavage to yield the hydroxamic acid, 8, but under the same conditions the sterically hindered 9 decomposes predominately by N-O bond cleavage with a pH independent rate constant that is 7.5-fold smaller than that for 7. In the pH range 0.5-7.0 three different processes for the decomposition of 9 were detected by kinetics. Only the process that dominates at neutral pH generates a nitrenium species that can be trapped by N3−. 相似文献
9.
Ronald Grigg Anne HodgsonJames Morris Visuvanathar Sridharan 《Tetrahedron letters》2003,44(5):1023-1026
A novel sequential palladium/ruthenium-catalysed four component process is described involving carbonylation of an aryl/heteroaryl iodide followed by allenylation to generate (π-allyl) palladium species which are intercepted by nitrogen nucleophiles to afford 1,6-dienes. Subsequent Ring-Closing Metathesis (RCM) affords C-acyl-N-heterocycles in good yield. These heterocycles proved to be active dipolarophiles in sequential and cascade 1,3-dipolar cycloaddition reactions (1,3-DC) as exemplified by reactions with nitrones and azomethine ylides. 相似文献
10.
Ronald Grigg William S. MacLachlan David T. MacPherson Visuvanathar Sridharan Selvaratnam Suganthan 《Tetrahedron》2001,57(52):10335-10345
Up to four bonds and five stereocentres are created, in five component processes (five point diversity), utilising resin bound aryl iodides by hydroboration or hydrostannylation of alkynes, followed by cyclisation–anion capture involving Suzuki or Stille reactions. Three small libraries were prepared to validate the chemistry. 相似文献