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71.
Sivacharan Kollipara Girish Bende Nitin Agarwal Brijesh Varshney Jyoti Paliwal 《Chromatographia》2011,73(3-4):201-217
US FDA released guidelines for bioanalytical method validation in 2001 and it became the basis for guidelines such as ANVISA and EMA. Even though there is a general agreement between these guidelines in terms of evaluation of validation parameters, significant diversity exists with respect to methodology employed. Present review compares and summarizes the regulatory guidelines issued by US FDA, ANVISA and EMA for bioanalytical method validation. This review also discusses evaluation of certain validation parameters such as matrix effect, incurred sample reanalysis, various stability aspects, effect of anticoagulant counter ions, specificity in the presence of concomitant medications, and identification of pharmacokinetic repeats wherein specific guidance and general consensus amongst scientific community does not exist. 相似文献
72.
Manisha Sharma Arti Maheshwari Nitin Bindal 《Journal of heterocyclic chemistry》2013,50(Z1):E116-E120
Some new derivatives of 3‐chloro‐1‐(4a,10b‐diazaphenanthrene‐2‐yl)‐4‐phenyl azetidin‐2‐one were synthesized through the reaction of N‐{4‐[phenyldiazenyl] phenyl}‐N‐[phenyl methylene] amine with 4‐[phenyldiazenyl] aniline. The resulting 3‐chloro‐4‐phenyl‐1‐{4‐[phenyldiazenyl] phenyl} azetidin‐2‐one intermediate in benzene was irradiated in a Pyrex vessel with 350 nm UV light in a photochemical reactor to give the desired derivatives (4a–j) . Structures of the new compounds were verified on the basis of spectral and elemental methods of analyses. Nine of the prepared compounds were tested for their anti‐inflammatory effects; most of these compounds showed potent and significant results compared with indomethacin. 相似文献
73.
Nitin D. Gaikwad Sachin V. Patil Vivek D. Bobade 《Journal of heterocyclic chemistry》2013,50(3):519-527
A series of new 1‐[4‐(2,3,4‐substituted‐phenyl) thiazol‐2‐yl]‐3‐(2,3,4‐substituted‐phenyl)‐1H‐pyrazole‐4‐carbaldehyde ( 4a , 4b , 4c , 4d , 4e , 4f , 4g , 4h , 4i , 4j , 4k , 4l , 4m ), 4‐[4‐(4‐substituted‐phenyl) thiazol‐2‐yl]‐3‐(4‐substituted‐phenyl)‐1‐phenyl‐1H‐pyrazole ( 7a , 7b , 7c , 7d , 7e , 7f , 7g , 7h , 7i ), 4‐[4‐(4‐substituted phenyl)thiazol‐2‐yl]‐1‐phenyl‐1H‐pyrazol‐3‐amine ( 10a , 10b , 10c , 10d , 10e , 10f , 10g ) have been synthesized by using Vilsmeier Haack formylation and Hantzsch reaction in high yield. All the synthesized compounds were tested qualitative (Zone of inhibition) and quantitative antimicrobial activities (MIC). Most of the synthesized compounds showed potent antimicrobial activity against gram positive and gram negative bacteria as well as fungi species. 相似文献
74.
Debosreeta Bose Deboleena Sarkar Nitin Chattopadhyay 《Photochemistry and photobiology》2010,86(3):538-544
In the present investigation, an attempt has been made to study the interaction of phenosafranin (PSF), a cationic phenazinium dye with the transport proteins, bovine serum albumin (BSA) and human serum albumin (HSA), employing steady-state and time-resolved fluorometric and circular dichroism (CD) techniques. The photophysical properties of the dye are altered on binding with the serum proteins. An explicit study with respect to the modification of the fluorescence and fluorescence anisotropy upon binding, effect of denaturant, fluorescence lifetime and CD measurements reveal that the dye binds to both BSA and HSA with almost the same affinity. Far-UV CD spectra indicate a decrease in the percentage of α-helicity only for BSA upon binding with the probe. Near-UV CD responses indicate an alteration in the tertiary structure of both the transport proteins because of binding. 相似文献
75.
Das P Mallick A Chakrabarty A Haldar B Chattopadhyay N 《The Journal of chemical physics》2006,125(4):44516
In continuation of our recent study on the steady state photophysics of a biologically active beta-carboline derivative, 3-acetyl-4-oxo-6,7-dihydro-12H indolo-[2,3-a] quinolizine (AODIQ), in the present article we have investigated the effect of nanocavity confinement on the excited state dynamics and rotational relaxation of the probe using picosecond time resolved fluorescence and fluorescence anisotropy techniques. The polarity dependent intramolecular charge transfer process is responsible for the remarkable sensitivity of this biological fluorophore in micellar environments. The fluorescence anisotropy decay of AODIQ incorporated inside the micelle is biexponential. The rotational motion of the probe was interpreted on the basis of a two step model consisting of a fast restricted rotation of the probe and a slow lateral diffusion of the probe in the micelle; both coupled to the overall rotation of the micelle. Experimental results reveal that micellar environment causes significant retardation of both the wobbling as well as the translational motion of the probe. 相似文献
76.
Chetan C. Chintawar Amit K. Yadav Nitin T. Patil 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(29):11906-11911
Herein, we disclose the gold-catalyzed 1,2-diarylation of alkenes through the interplay of ligand-enabled AuI/AuIII catalysis with the idiosyncratic π-activation mode of gold complexes. Unlike the classical migratory-insertion-based approach to 1,2-diarylation, the present approach not only circumvents the formation of direct Ar−Ar′ coupling and Heck-type side products but more intriguingly demonstrates reactivity and selectivity complementary to those of previously known metal catalysis (Pd, Ni, or Cu). Detailed investigations to underpin the mechanistic scenario revealed oxidative addition of aryl iodides to an AuI complex to be the rate-limiting step owing to the non-innocent nature of the aryl alkene. 相似文献
77.
Chetan C. Chintawar Amit K. Yadav Nitin T. Patil 《Angewandte Chemie (International ed. in English)》2020,59(29):11808-11813
Herein, we disclose the gold‐catalyzed 1,2‐diarylation of alkenes through the interplay of ligand‐enabled AuI/AuIII catalysis with the idiosyncratic π‐activation mode of gold complexes. Unlike the classical migratory‐insertion‐based approach to 1,2‐diarylation, the present approach not only circumvents the formation of direct Ar?Ar′ coupling and Heck‐type side products but more intriguingly demonstrates reactivity and selectivity complementary to those of previously known metal catalysis (Pd, Ni, or Cu). Detailed investigations to underpin the mechanistic scenario revealed oxidative addition of aryl iodides to an AuI complex to be the rate‐limiting step owing to the non‐innocent nature of the aryl alkene. 相似文献
78.
Nitin Kumar Dr. Rapelly Venkatesh Prof. Sundaram Singh Prof. Jeyakumar Kandasamy 《European journal of organic chemistry》2023,26(37):e202300679
An efficient and eco-friendly method has been developed for the preparation of functionalized 3-(S)-arylthioindoles in good to excellent yields from indoles and aryl thiols in water. The coupling reaction was prompted by K2S2O8 in the presence of glucose at room temperature. Broad substrate scope, functional group tolerance, room temperature reactions and metal-free conditions are the salient features of the developed methodology. 相似文献
79.
80.
Ladislav Skula 《Czechoslovak Mathematical Journal》2009,59(3):759-771
On the ring R = F[x 1,..., x n ] of polynomials in n variables over a field F special isomorphisms A’s of R into R are defined which preserve the greatest common divisor of two polynomials. The ring R is extended to the ring S: = F[[x 1,..., x n ]]+ and the ring T: = F[[x 1,..., x n ]] of generalized polynomials in such a way that the exponents of the variables are non-negative rational numbers and rational numbers, respectively. The isomorphisms A’s are extended to automorphisms B’s of the ring S. Using the property that the isomorphisms A’s preserve GCD it is shown that any pair of generalized polynomials from S has the greatest common divisor and the automorphisms B’s preserve GCD. On the basis of this Theorem it is proved that any pair of generalized polynomials from the ring T = F[[x 1,..., x n ]] has a greatest common divisor. 相似文献