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751.
752.
Various aliphatic hydrocarbons and the side chains of aromatic hydrocarbons were chlorinated in subcritical carbon tetrachloride. Chlorination of aromatic compounds including 1,4-disubstituted benzenes was investigated. Ketones and sulfones were stable under the employed conditions. Sulfoxides were converted into sulfides in a low to modest yields. The coupling adducts between olefins and carbon tetrachloride were obtained from the reactions of olefins. 相似文献
753.
Li CZ Matsuo Y Niinomi T Sato Y Nakamura E 《Chemical communications (Cambridge, England)》2010,46(45):8582-8584
Treatment of [60]fullerene with potassium methylnaphthalenide and excess C(6)F(5)CH(2)Br afforded 1,4-bis(pentafluorobenzyl)[60]fullerene, the study of which showed that there is a face-to-face interaction between [60]fullerene and a perfluoro aromatic ring, allowing the molecule to be utilized for high-performance organic photovoltaic devices. 相似文献
754.
Nishida H Mukaihira T Saitoh F Harada K Fukui M Matsusue T Okamoto A Hosaka Y Matsumoto M Shiromizu I Ohnishi S Mochizuki H 《Chemical & pharmaceutical bulletin》2004,52(4):406-412
In the course of development of factor Xa (FXa) inhibitor in an investigation involving the synthesis of 1-arylsulfonyl-3-piperazinone derivatives, we found new compounds containing a unique spiro skeleton. Among such compounds, (-)-7-[(6-chloro-2-naphthalenyl)sulfonyl]tetrahydro-8a-(methoxymethyl)-1'-(4-pyridinyl)-spiro[5H-oxazolo[3,2-a]pyrazine-2(3H),4'-piperidin]-5-one (28, M55529) had activity more favorable than those of previously reported compounds. The inhibitory activity of M55529 for FXa is IC(50)=2 nM, with high selectivity for FXa over thrombin and trypsin. 相似文献
755.
Shin-ichi Hirashima Takaaki Sakai Kosuke Nakashima Nana Watanabe Yuji Koseki Kanako Mukai Yohei Kanada Norihiro Tada Akichika Itoh Tsuyoshi Miura 《Tetrahedron letters》2014
Diaminomethylenemalononitrile organocatalyst 1 efficiently promotes the asymmetric conjugate addition of malonates to α,β-unsaturated ketones to afford the corresponding addition products in high to excellent yields with up to 98% ee. 相似文献
756.
Chemoselective Reductive Nucleophilic Addition to Tertiary Amides,Secondary Amides,and N‐Methoxyamides 下载免费PDF全文
Minami Nakajima Yukiko Oda Takamasa Wada Ryo Minamikawa Dr. Kenji Shirokane Dr. Takaaki Sato Noritaka Chida 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(52):17565-17571
As the complexity of targeted molecules increases in modern organic synthesis, chemoselectivity is recognized as an important factor in the development of new methodologies. Chemoselective nucleophilic addition to amide carbonyl centers is a challenge because classical methods require harsh reaction conditions to overcome the poor electrophilicity of the amide carbonyl group. We have successfully developed a reductive nucleophilic addition of mild nucleophiles to tertiary amides, secondary amides, and N‐methoxyamides that uses the Schwartz reagent [Cp2ZrHCl]. The reaction took place in a highly chemoselective fashion in the presence of a variety of sensitive functional groups, such as methyl esters, which conventionally require protection prior to nucleophilic addition. The reaction will be applicable to the concise synthesis of complex natural alkaloids from readily available amide groups. 相似文献
757.
Two of each diastereomers of the C-1-C-10 and C-17-C-29 segments of amphidinolide C (1) were synthesized. Comparing the 1H NMR chemical shifts of its MTPA esters with those of linear methyl ester of 1, the absolute configurations at C-7, C-8, C-20, C-23, and C-24 in amphidinolide C (1) were confirmed to be all R. 相似文献
758.
Yasuda T Yoshimura Y Yabuki H Nakazawa T Ohsawa K Mimaki Y Sashida Y 《Chemical & pharmaceutical bulletin》2003,51(12):1426-1428
During the course of our systematic investigation of the metabolism of flavonoids, the polymethoxyflavone nobiletin, occurring in the fruits of Citrus depressa, was orally administered to rats. The urinary metabolites were separated and identified by three-dimensional HPLC equipped with a photodiode array detector and the structure was determined by spectroscopic methods to be 4'-hydroxy-3',5,6,7,8-pentamethoxyflavone (1). 相似文献
759.
Shizuka Anan Yumi Mochizuki Kenta Kokado Kazuki Sada 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(24):8102-8107
The A–A/B–B step‐growth copolymerization between a monomer immobilized in the crystalline state and a monomer mobile in the solution state is demonstrated. One of the two monomers was immobilized as organic ligands of the metal–organic framework (MOF) and polymerized with the mobile guest monomer, resulting in the formation of linear polymers. The polymerization behavior was completely different from that of the solution polymerizations. In particular, the degrees of polymerization (DP) converged to a specific value depending on the MOF structures. The inevitable termination is caused not by imperfectness of the polymerization reaction, but by the selection of the two polymerization partners among the several adjacent immobilized monomers. This is fully supported by the Monte Carlo simulation on the basis of the polymerization mechanism. Precise immobilization of monomers in the supramolecular assemblies is a promising way for the controlled A–A/B–B step‐growth polymerization. 相似文献
760.
Takaaki Kawaguchi Fumio Sanda Toshio Masuda 《Journal of polymer science. Part A, Polymer chemistry》2002,40(22):3938-3943
The polymerization of isobutyl vinyl ether (IBVE) and tert‐butyl vinyl ether (TBVE) was carried out with metallocene and nonmetallocene catalysts, and the stereoregularity of the formed polymers was examined with 13C NMR spectroscopy. IBVE afforded polymers with 63–68% dyad isotacticity by polymerization with mixtures of metallocene catalysts and methyl aluminoxane as a cocatalyst in toluene as a solvent. However, TBVE yielded polymers with 47–52% dyad isotacticity (21–28% triad isotacticity) under the same conditions, the isotacticity being lower than that of poly(isobutyl vinyl ether) (PIBVE). Nonmetallocene catalysts, including Ti, Zr, and Hf complexes with two phenoxy imine chelate ligands, provided PIBVE and poly(tert‐butyl vinyl ether) with 63–68 and 45–51% dyad isotacticity, respectively. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 40: 3938–3943, 2002 相似文献