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排序方式: 共有197条查询结果,搜索用时 78 毫秒
101.
K Sakakibara LA Joyce T Mori T Fujisawa SH Shabbir JP Hill EV Anslyn K Ariga 《Angewandte Chemie (International ed. in English)》2012,51(38):9643-9646
Push a host: Mechanical compression was applied to a host monolayer at an interface, which facilitated an indicator displacement assay. The fluorescence resonance energy transfer (FRET) between the host and indicator was switched on by this compression. Addition of D-glucose caused the indicator to be displaced, effectively quenching the FRET process. 相似文献
102.
Kazunori Tsubaki Masahide Sakakibara Yuki Nakatani Takeo Kawabata 《Tetrahedron》2006,62(44):10321-10324
The efficient functionalization of three upper rims based on Suzuki-Miyaura coupling to temporarily lower rim-protected hexahomotrioxacalix[3]arenes was developed. After deprotection of the three protecting groups, the three upper rim-functionalized and lower rim-free hexahomotrioxacalix[3]arenes 5a-5m were synthesized. 相似文献
103.
Onimaru T Matsumoto KT Inoue YF Umeo K Sakakibara T Karaki Y Kubota M Takabatake T 《Physical review letters》2011,106(17):177001
An antiferroquadrupolar ordering at T(Q)=0.11 K has been found in a Pr-based superconductor PrIr(2)Zn(20). The measurements of specific heat and magnetization revealed the non-Kramers Γ(3) doublet ground state with the quadrupolar degrees of freedom. The specific heat exhibits a sharp peak at T(Q)=0.11 K. The increment of T(Q) in magnetic fields and the anisotropic B-T phase diagram are consistent with the antiferroquadrupolar ordered state below T(Q). The entropy release at T(Q) is only 20% of Rln2, suggesting that the quadrupolar fluctuations play a role in the formation of the superconducting pairs below T(c)=0.05 K. 相似文献
104.
Dr. Tsubasa Inokuma Takuya Sakakibara Takatoshi Someno Kana Masui Dr. Akira Shigenaga Prof. Dr. Akira Otaka Prof. Dr. Ken-ichi Yamada 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(60):13829-13832
A practical method for synthesizing chiral α-amino phosphonic acid derivatives was developed. Readily available and stable N-o-nitrophenylsulfenyl (Nps) imino phosphonate was utilized as a substrate for a highly enantioselective Friedel–Crafts-type addition of indole or pyrrole nucleophiles catalyzed by chiral phosphoric acid. The resulting adduct was easily converted into N-9-fluorenylmethyloxycarbonyl (Fmoc) amino phosphonic acid, which is useful for synthesizing peptides containing an amino phosphonic acid. 相似文献
105.
Dr. Yusuke Takezawa Shiori Sakakibara Prof. Dr. Mitsuhiko Shionoya 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(67):16626-16633
DNA three-way junction (3WJ) structures are essential building blocks for the construction of DNA nanoarchitectures. We have synthesized a bipyridine (bpy)-modified DNA 3WJ by using a newly designed bpy-modified nucleoside, Ubpy- 3 , in which a bpy ligand is tethered via a stable amide linker. The thermal stability of the bpy-modified 3WJ was greatly enhanced by the formation of an interstrand NiII(bpy)3 complex at the junction core (ΔTm=+17.7 °C). Although the stereochemistry of the modification site differs from that of the previously reported bpy-modified nucleoside Ubpy- 2 , the degree of the NiII-mediated stabilization observed with Ubpy- 3 was comparable to that of Ubpy- 2 . Structure induction of the 3WJs and the duplexes was carried out by the addition or removal of NiII ions. Furthermore, NiII-mediated self-sorting of 3WJs was performed by using the bpy-modified strands and their unmodified counterparts. Both transformations were driven by the formation of NiII(bpy)3 complexes. The structural induction and self-sorting of bpy-modified 3WJs are expected to have many potential applications in the development of metal-responsive DNA materials. 相似文献
106.
Skeletal muscle atrophy is the decrease in muscle mass and strength caused by reduced protein synthesis/accelerated protein degradation. Various conditions, such as denervation, disuse, aging, chronic diseases, heart disease, obstructive lung disease, diabetes, renal failure, AIDS, sepsis, cancer, and steroidal medications, can cause muscle atrophy. Mechanistically, inflammation, oxidative stress, and mitochondrial dysfunction are among the major contributors to muscle atrophy, by modulating signaling pathways that regulate muscle homeostasis. To prevent muscle catabolism and enhance muscle anabolism, several natural and synthetic compounds have been investigated. Recently, polyphenols (i.e., natural phytochemicals) have received extensive attention regarding their effect on muscle atrophy because of their potent antioxidant and anti-inflammatory properties. Numerous in vitro and in vivo studies have reported polyphenols as strongly effective bioactive molecules that attenuate muscle atrophy and enhance muscle health. This review describes polyphenols as promising bioactive molecules that impede muscle atrophy induced by various proatrophic factors. The effects of each class/subclass of polyphenolic compounds regarding protection against the muscle disorders induced by various pathological/physiological factors are summarized in tabular form and discussed. Although considerable variations in antiatrophic potencies and mechanisms were observed among structurally diverse polyphenolic compounds, they are vital factors to be considered in muscle atrophy prevention strategies. 相似文献
107.
108.
J. Happel S. Umemura Y. Sakakibara H. Blanck und S. Kunichika 《Colloid and polymer science》1977,255(5):513
Ohne Zusammenfassung 相似文献
109.
Arnebinol, a new ansa-type prenylated phenol, was synthesized in 12 steps from geraniol and p-benzoquinone in 5.1 % overall yield. 相似文献
110.