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121.
A Combined Experimental and Computational Study on the Cycloisomerization of 2‐Ethynylbiaryls Catalyzed by Dicationic Arene Ruthenium Complexes
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Prof. Dr. Yoshihiko Yamamoto Kazuma Matsui Dr. Masatoshi Shibuya 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(19):7245-7255
Ruthenium‐catalyzed cycloisomerization of 2‐ethynylbiaryls was investigated to identify an optimal ruthenium catalyst system. A combination of [η6‐(p‐cymene)RuCl2(PR3)] and two equivalents of AgPF6 effectively converted 2‐ethynylbiphenyls into phenanthrenes in chlorobenzene at 120 °C over 20 h. Moreover, 2‐ethynylheterobiaryls were found to be favorable substrates for this ruthenium catalysis, thus achieving the cycloisomerization of previously unused heterocyclic substrates. Moreover, several control experiments and DFT calculations of model complexes were performed to propose a plausible reaction mechanism. 相似文献
122.
Real-root property of the spectral polynomial of the Treibich–Verdier potential and related problems
Zhijie Chen Ting-Jung Kuo Chang-Shou Lin Kouichi Takemura 《Journal of Differential Equations》2018,264(8):5408-5431
We study the spectral polynomial of the Treibich–Verdier potential. Such spectral polynomial, which is a generalization of the classical Lamé polynomial, plays fundamental roles in both the finite-gap theory and the ODE theory of Heun's equation. In this paper, we prove that all the roots of such spectral polynomial are real and distinct under some assumptions. The proof uses the classical concept of Sturm sequence and isomonodromic theories. We also prove an analogous result for a polynomial associated with a generalized Lamé equation, where we apply a new approach based on the viewpoint of the monodromy data. 相似文献
123.
Yue-Wei Ge Shu Zhu Kohei Kazuma Sheng-Li Wei Kayo Yoshimatsu Katsuko Komatsu 《Analytical and bioanalytical chemistry》2016,408(13):3555-3570
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125.
Takumi Nakamura Kazuma Ban Dr. Yasushi Yoshida Prof. Dr. Takashi Mino Prof. Dr. Yoshio Kasashima Prof. Dr. Masami Sakamoto 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(66):16338-16341
Asymmetric synthesis was performed by combining the photochemical reaction of an achiral substrate followed by crystallization-induced deracemization. The results indicated that a fused indoline produced by photochemical intramolecular δ-hydrogen abstraction and cyclization of N-(5-chloro-2-methylphenyl)phthalimide crystallized as a racemic conglomerate. Since this substrate has an aminal skeleton, racemization involving a ring-opening and ring-closing equilibrium process occurred under suitable conditions. Efficient racemization was observed in acetone containing a catalytic base, 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU). Crystallization-induced dynamic deracemization by Viedma ripening from racemic indoline was performed with an excellent enantioselectivity of 99 % ee. Furthermore, one-pot asymmetric synthesis of the indoline was achieved by the photochemical reaction of achiral phthalimide followed by continuous attrition-enhanced deracemization converging to 99 % ee of enantiomeric crystals. This is the first example of asymmetric expression and amplification by photochemical hydrogen abstraction and crystallization-induced dynamic deracemization. 相似文献
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127.
Sie Tiong Ha Kok Leei Foo Hong Cheu Lin Masato M.Ito Kazuma Abe Kenji Kunbo S.Sreehari Sastry 《中国化学快报》2012,23(7):761-764
正A homologous series of heterocycles,6-methyl-2-(4-alkoxybenzylidenamino)benzothiazoles,were synthesized and characterized using FT-IR,~1H and ~(13)C NMR and mass spectrometric analysis.Enantiotropic nematic phase was observed for shorter members.Smectic A phase only emerged from octyloxy derivative onwards.The terminal methyl group at the benzothiazole fragment and the Schiff base linkage influenced the mesomorphic behavior of the present series. 相似文献
128.
Synthesis of Triarylpyridines in Thiopeptide Antibiotics by Using a C−H Arylation/Ring‐Transformation Strategy
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Kazuma Amaike Prof. Dr. Kenichiro Itami Prof. Dr. Junichiro Yamaguchi 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(13):4384-4388
We have described a C?H arylation/ring‐transformation strategy for the synthesis of triarylpyridines, which form the core structure of thiopeptide antibiotics. This synthetic method readily gave 2,3,6‐triarylpyridines in a regioselective manner by a two‐phase approach: C?H arylation (a nickel‐catalyzed decarbonylative Suzuki–Miyaura cross‐coupling and decarbonylative C?H coupling for the synthesis of 2,4‐diaryloxazoles) and ring transformation ([4+2] cycloaddition of 2,4‐diaryloxazoles with (hetero)arylacrylic acids). To showcase these methods, we have accomplished the formal synthesis of thiopeptide antibiotics GE2270 s and amythiamicins. 相似文献
129.
Yusuke Ishigaki Takumi Hashimoto Kazuma Sugawara Shuichi Suzuki Takanori Suzuki 《Angewandte Chemie (International ed. in English)》2020,59(16):6581-6584
Thermally switchable redox properties have been reported to be due to a change in the spin state of newly designed overcrowded ethylenes, which can adopt closed‐shell folded and open‐shell twisted forms. In this study, tetrathienylanthraquinodimethane derivatives were designed to be in thermal equilibrium between a more stable folded form and less stable but more donating twisted diradical in solution, so that the oxidation potential can be controlled by heating/cooling. This is the first example of a switching of redox properties based on a thermally equilibrated twisted diradical, which can be more readily oxidized to the twisted dication. 相似文献
130.