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81.
Kenji Mori 《Bioscience, biotechnology, and biochemistry》2013,77(10):2045-2047
A key intermediate, 2-isocyano-3-hydroxybutyrate (III) was isolated from a reaction of isocyanoacetate (I) with acetaldehyde (II) in the presence of Et3N. It was found that III was readily converted into 2-isocyanocrotonate (V) and 2-isocyano-2-(1′-hydroxyethyl)-3-hydroxybutyrate (VI) which are undesirable compounds for the synthesis of threonine. However, by use of a metal catalyst (e.g. NiCl2 or PdCl2), the isocyano-hydroxy compound (III) was selectively converted into 5-methyl-4-alkoxycarbonyl-2-oxazoline (IV) which is an important precursor of threonine. Furthermore, chemical properties of IV were examined; the results suggested that cis-oxazoline was relatively sensitive to acid, base and heat.On the basis of these results, the reaction of I with II was carried out using Et3N-PdCl2 as a catalyst to obtain threo-threonine (85% purity) in a good yield (85%). 相似文献
82.
Michinori Nakamura 《Bioscience, biotechnology, and biochemistry》2013,77(5):398-405
The properties of UDPG → fructose transglucosylase, partially purified from immature soybeans or broad beans, were investigated. Magnesium ions had a stimulating effect on this enzyme. Evidence was presented to show that UDPG, the glucosyl group donor for sucrose synthesis, was regenerated from UDP and G-1-P in the presence of ATP. 相似文献
83.
The structure of cercosporin, a deep red photosensitizing pigment isolated from the cultured mycelia of Cercospora kikuchii (Matsumoto et Tomoyasu) Gardner, has been elucidated as 1,12-bis(2-hydroxypropyl)-2,11-dimethoxy-6,7-methylenedioxy-4,9-dihydroxyperylene-3,10-quinone(Ia). All substituents are symmetrically arranged and the molecule has a two-fold rotation axis. An unusual seven-membered methylenedioxy bridged system endows the molecule with the inherently dissymmetric nature. Isocercosporin(Ib), a stereoisomer of Ia, was separated and the stereochemistry and the molecular dissymmetry of both isomers were also discussed. 相似文献
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Takemitsu Mizunaga Tadahiro Oshida Akiko Takasaki Yoshiharu Maruyama 《Bioscience, biotechnology, and biochemistry》2013,77(6):1445-1450
To find the function of the mannan chains covalently attached to yeast repressible acid phosphatase, the N-glycosidic carbohydrate chains were removed by endo-β-N-acetyl-glucosaminidase H under native conditions. Almost all of the N-glycosidic mannan chains were cleaved off by the glycosidase. The deglycosylated enzyme was shown to be a dimer structure as is the native enzyme. The deglycosylated enzyme retained enzyme activity, the same Km, and the same circular dichroism spectra as the native enzyme. These results indicate that the carbohydrate chains are not essential for maintaining the active enzyme structure, but the deglycosylated enzyme was shown to be more sensitive to acidic pH and high temperature. 相似文献
87.
Keiji Harashima Nobuo Tsuchida Teruo Tanaka Junsaku Nagatsu 《Bioscience, biotechnology, and biochemistry》2013,77(4):481-489
A water-insoluble red antibiotic pigment was isolated from mycelia of a strain of Streptomyces. It was found that the pigment is a new C25-prodigiosin-analogue and the authors propose to designate it prodigiosin-25 C. The chemical structure (XI) has been deduced from visible absorption spectra, NMR spectra, mass spectra and analysis of degradation products of the pigment. 相似文献
88.
Targeting of extracellular protein–protein interactions (PPI) is emerging as a major application for de novo discovered macrocyclic peptides. Modern discovery platforms can routinely identify macrocyclic peptide ligands capable of highly selective modulation of extracellular signaling pathways; amenability to chemical synthesis and natural modularity of peptides additionally provides an avenue for their further structural elaboration, while the challenge of cell internalization can be minimized. Here, we discuss the recent progress in targeting extracellular PPIs with macrocyclic peptides by focusing on a number of recent case studies. We analyze the scope and potential limitations of the discovery systems in identifying functional macrocyclic ligands. We also highlight the recent technical advancements allowing for a more streamlined discovery pipeline and our brief perspective in this field. 相似文献
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The occurrence of a new brassinosteroid of (22S,24R)-3β,22-dihydroxy-5α-ergostan-6-one, named cathasterone, was demonstrated by a GC-MS analysis in cultured cells of Catharanthus roseus. Its endogenous level was in the range of 2–4 ng/g fw, similar to those of brassinolide and castasterone. A feeding experiment with a deuterium-labeled substrate revealed that cathasterone was converted to teasterone and typhasterol. This is the first report of the natural occurrence of cathasterone as a brassinosteroid being the biosynthetic precursor of teasterone. 相似文献