全文获取类型
收费全文 | 745篇 |
免费 | 22篇 |
国内免费 | 1篇 |
专业分类
化学 | 636篇 |
晶体学 | 11篇 |
力学 | 7篇 |
数学 | 28篇 |
物理学 | 86篇 |
出版年
2023年 | 3篇 |
2022年 | 4篇 |
2021年 | 6篇 |
2020年 | 5篇 |
2019年 | 6篇 |
2018年 | 4篇 |
2017年 | 8篇 |
2016年 | 10篇 |
2015年 | 16篇 |
2014年 | 11篇 |
2013年 | 33篇 |
2012年 | 24篇 |
2011年 | 34篇 |
2010年 | 28篇 |
2009年 | 28篇 |
2008年 | 67篇 |
2007年 | 51篇 |
2006年 | 54篇 |
2005年 | 40篇 |
2004年 | 51篇 |
2003年 | 45篇 |
2002年 | 61篇 |
2001年 | 9篇 |
2000年 | 12篇 |
1999年 | 11篇 |
1998年 | 9篇 |
1997年 | 6篇 |
1996年 | 12篇 |
1995年 | 5篇 |
1994年 | 5篇 |
1993年 | 3篇 |
1992年 | 5篇 |
1989年 | 4篇 |
1988年 | 4篇 |
1987年 | 2篇 |
1986年 | 3篇 |
1985年 | 13篇 |
1984年 | 15篇 |
1983年 | 4篇 |
1982年 | 10篇 |
1981年 | 6篇 |
1980年 | 4篇 |
1979年 | 4篇 |
1978年 | 4篇 |
1977年 | 4篇 |
1976年 | 8篇 |
1973年 | 7篇 |
1969年 | 2篇 |
1967年 | 1篇 |
1964年 | 1篇 |
排序方式: 共有768条查询结果,搜索用时 312 毫秒
81.
Matsuda H Nakamura S Fujimoto K Moriuchi R Kimura Y Ikoma N Hata Y Muraoka O Yoshikawa M 《Chemical & pharmaceutical bulletin》2010,58(12):1617-1621
The methanolic extract and its 1-butanol-soluble fraction from the flower buds of Camellia sasanqua THUNB. were found to show inhibitory activities on the release of β-hexosaminidase from rat basophile leukemia (RBL-2H3) cells. From the 1-butanol-soluble fraction, five new acylated oleanane-type triterpene saponins, sasanquasaponins I-V, were isolated together with a known saponin and their chemical structures were elucidated on the basis of chemical and physicochemical evidence. The principal saponin constituents, sasanquasaponins I-III, with an acyl group at the 22-position of the aglycon part showed the inhibitory effects on the release of β-hexosaminidase and some structure-activity relationships were reported. 相似文献
82.
Yoshinao Kumagai Yuuki Enatsu Masanari Ishizuki Yuki Kubota Jumpei Tajima Toru Nagashima Hisashi Murakami Kazuya Takada Akinori Koukitu 《Journal of Crystal Growth》2010,312(18):2530-2536
Void formation at the interface between thick AlN layers and (0 0 0 1) sapphire substrates was investigated to form a predefined separation point of the thick AlN layers for the preparation of freestanding AlN substrates by hydride vapor phase epitaxy (HVPE). By heating 50–200 nm thick intermediate AlN layers above 1400 °C in a gas flow containing H2 and NH3, voids were formed beneath the AlN layers by the decomposition reaction of sapphire with hydrogen diffusing to the interface. The volume of the sapphire decomposed at the interface increased as the temperature and time of the heat treatment was increased and as the thickness of the AlN layer decreased. Thick AlN layers subsequently grown at 1450 °C after the formation of voids beneath the intermediate AlN layer with a thickness of 100 nm or above self-separated from the sapphire substrates during post-growth cooling with the aid of voids. The 79 μm thick freestanding AlN substrate obtained using a 200 nm thick intermediate AlN layer had a flat surface with no pits, high optical transparency at wavelengths above 208.1 nm, and a dislocation density of 1.5×108 cm−2. 相似文献
83.
Yasuhiro Kajihara Hironobu Hashimoto Hisashi Kodama Tomio Wakabayashi Ken-ichi Sato 《Journal of carbohydrate chemistry》2013,32(7):991-995
Abstract Specific inhibitors of glycosyltransferases have become of interest1 not only for investigation of carbohydrate-participating cell-surface phenomena but also for practical use such as chemotherapeutic reagents. Glycosyltransferases catalyze the transfer of glycosyl moieties from nucleotide donors to oligosaccharide acceptors. Therefore, two kinds of substrate-analog inhibitors are possible. The donor analogs have been rather well studied, but are not specific. On the other hand, glycosyltransferases have in general smct acceptor specifkity. Recently, acceptor analogs which inhibit the corresponding glycosyltransferases were reported2-5 and as expected were acceptor-specific inhibitors. 相似文献
84.
Keitaro Tanoi Natsuko I. Kobayashi Takayuki Saito Naoko Iwata Atsushi Hirose Yoshimi Ohmae Ren Iwata Hisashi Suzuki Tomoko M. Nakanishi 《Journal of Radioanalytical and Nuclear Chemistry》2013,296(2):749-751
The time course of Mg uptake and release using intact rice plants and 28Mg as a tracer is presented. Since there is no conventional Mg tracer available, 28Mg was produced via 27Al(α, 3p)28Mg reaction using a cyclotron. Using the purified 28Mg tracer, it was found that the uptake amount of 28Mg by the rice plants increased linearly during 30 min of application. After 28Mg treatment for 90 min, the roots were sequentially washed with iced solution for 120 min. Within about 10 min, almost all of the 28Mg, that was thought to be weakly bound to the apoplast, was washed away. 相似文献
85.
86.
In considering the retailer–supplier supply chain, this paper analyzes how a retailer reasonably decides both the depth and frequency of the price discount promotion including or excluding a supplier’s inventory decision. Assuming that the promotion frequency used by the retailer is probabilistic, we model a promotion-inventory decision under an AR(1) demand with a Markov switching promotion regime. After obtaining the optimal promotion plan, our analysis also considers the behavior of the optimal promotion decision; the retailer’s price format selection, either an Every-Day-Low-Price policy (EDLP) or a Promotion policy (HiLo); and the impact of information sharing of promotion status on the system’s performance. Our results suggest that a retailer tends to overpromote if inventory cost is excluded in its promotion decision, that increasing the market share is a preferable action for both the retailer and the supplier, that total margin and price-elasticity play an important role in selecting the price format, and that the profitability for a supplier of sharing promotion information depends on the transition probabilities of the Markov switching regime. 相似文献
87.
Katsunori Watabe Hisashi Kanda Katsuya Sato Toshiyuki Hobo 《Journal of chromatography. A》1992,590(2):289-296
In continuous counter-current gas-liquid chromatography, which has a high resolving power and is suitable for the large-scale purification of organic solvents, it is very important that the samples that can be applied extend from easily separable to more difficult to separate, such as azeotropes, low-volatility compounds and stereoisomers. A system was designed and constructed for high-temperature operation up to 200°C, and was applied to the separation of dimethyl and diethyl phthalate, trans- and cis-decahydronaphthalene and cis-decahydronaphthalene and tetrahydronaphthalene. It was confirmed that over 99% of purity could be achieved for dimethyl and diethyl phthalate, trans-decahydronaphthalene, and tetrahydronaphthalene. 相似文献
88.
Dr. Atsuto Izumiseki Prof. Dr. Hisashi Yamamoto 《Angewandte Chemie (International ed. in English)》2015,54(30):8697-8699
Selective Michael reaction of organolithium reagents to supersilyl methacrylate is reported. The method was able to control a single and double Michael addition. The successful termination of the process using the supersilyl protecting group allows for the controlled, chemoselective, and diastereoselective Michael reaction. 相似文献
89.
90.
Dr. Ramesh C. Samanta Prof. Hisashi Yamamoto 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(34):11976-11979
Electrophilic halogenation is used to produce a wide variety of halogenated compounds. Previously reported methods have been developed mainly using a reagent‐based approach. Unfortunately, a suitable “catalytic” process for halogen transfer reactions has yet to be achieved. In this study, arylamines have been found to generate an N‐halo arylamine intermediate, which acts as a highly reactive but selective catalytic electrophilic halogen source. A wide variety of heteroaromatic and aromatic compounds are halogenated using commercially available N‐halosuccinimides, for example, NCS, NBS, and NIS, with good to excellent yields and with very high selectivity. In the case of unactivated double bonds, allylic chlorides are obtained under chlorination conditions, whereas bromocyclization occurs for polyolefin. The reactivity of the catalyst can be tuned by varying the electronic properties of the arene moiety of catalyst. 相似文献