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81.
A New Furostanol Saponin from Dioscorea futshauensis 总被引:1,自引:0,他引:1
A new furostanol saponin presenting moderate bioacitivity of inducting morphological deformation of Pyricularia oryzae mycelia was isolated from Dioscorea futshauensis R.Kunth by bioacitivity-guided fractionation. The structure was established as 26-O-β-D-glucopyranosyl-3β,26-diol-23(S)-methoxyl-(25R)-furost-5,20(22)-diene-3-O-[α-L-rhamnopyranosyl(1→2)-β-D-glucopyranosyl(1→3)]-β-D-glucopyranoside on the basis of chemical evidencesand spectral analysis,especially by 2D-NMR techniques. 相似文献
82.
Two New Steroidal Glycosides from Liriope muscari 总被引:4,自引:0,他引:4
Zhi Hong CHENG Tao WU Yin Long GUO Bo Yang YU Luo Shan XU 《中国化学快报》2006,17(1):31-34
Liriope muscari (Decn.) Bailey (Liliaceae) is a folk medicinal plant used as a substitute of Ophiopogon japonicus (Thunb.) Ker-Gawl., mainly distributing in Quanzhou, Fujian Province, China1. Previously, we reported the isolation and identification of two… 相似文献
83.
Quinone-dependent pyranose dehydrogenase presents a new tool for versatile conversions of numerous carbohydrates to their di- and tricarbonyl derivatives. This enzyme purified from the basidiomycete Agaricus meleagris catalysed dioxidation of several aromatic β-d-glucopyranosides and a β-d-xylopyranoside into the corresponding 3,4-didehydro-β-d-aldopyranosides (β-d-aldopyranosid-3,4-diuloses) in high yields, typically >80% for 4-nitrophenyl glycosides. These new compounds were doubly hydrated in aqueous solution. According to in situ NMR investigations, the reaction intermediates were the corresponding 3- and 4-dehydro compounds. The analogous anomeric α-glycosides underwent one-step oxidation only at C-3 to 3-dehydro-α-d-aldopyranosides (α-d-pyranosid-3-uloses). 相似文献
84.
石香薷中两个新黄酮甙的研究 总被引:4,自引:0,他引:4
石香薷中两个新黄酮甙的研究郑尚珍,孙丽萍,沈序维王毅(西北师范大学化学系,兰州,730070)(中国科学院兰州化学物理研究所)关键词石香薷,唇形科,黄酮甙唇形科植物石香薷(MOslachinensisMaxim)作为中药,用来治疗暑湿感冒、头痛、腹痛... 相似文献
85.
K. J. Kucherbaev K. K. Uteniyazov V. V. Kachala Z. Saatov A. S. Shashkov 《Chemistry of Natural Compounds》2002,38(2):175-178
The known compound oleanolic acid (1) and a new cycloartane glycoside cyclounifolioside A (2), which has the structure 6,16-di-O-acetyl-24R-cycloartan-6,16,24,25-pentaol 3-O--D-glucopyranoside, were isolated from Astragalus unifoliolatus Bunge. The structures of the isolated compounds were established using chemical transformations and two-dimensional spectra (TOCSY, ROESY, HMBC, HSQC, COSY). 相似文献
86.
Hua Han Yang Hua Yi Ling Li Xiao Hua Wang Bao Shu Liu Peng Sun Min Xiang Pan Research Center for Marine Drugs School of Pharmacy Second Military Medical University Shanghai China 《中国化学快报》2007,18(2):161-164
A new triterpene glycoside, leucospilotaside A, along with a known saponin, isolated from sea cucumber Holothuria leucospilota, and its structure was elucidated as 3β-O-[4-O-sodiumsulfate-β-D-quinovopyranosyl-(1→2)-β-D-xylopyranosyl]-holosta-22-ketone-9-en-17α,25α-diol (1) by extensive spectroscopic analysis and chemical methods. Leucospilotaside A (1) has a ketone carbonyl group (22) in the aglycon side chain. 相似文献
87.
A new phenolic constituent along with five known compounds were isolated from Fagopyrum dibotrys(D.Don)Hara.The new compound was characterized as 1,3-dimethoxy-2-O-β-xylo-pyranosyl-5-O-β-glucopyranosyl-benzene,by spectroscopic analysis and enzymatic hydrolysis. 相似文献
88.
Shan-Shan Zhang Ri-Zhen Huang Cheng-Cheng Gong Lan-Ju Ji Hong-Fa Sun 《Natural product research》2018,32(6):668-675
Chemical investigation of the ethanolic extracts of the dried leaves of Bergenia purpurascens led to the isolation and identification of a new aromatic glycoside, 1-O-β-D-glucopyranosyl-2-methoxy-3-hydroxyl-phenylethene (1), along with other 19 known compounds (2–20). The structure of compound 1 was determined by a detailed analysis using various analytical techniques, including 1D and 2D NMR. In vitro anti-proliferative activities of compound 1 on five human cancer cell lines were evaluated. The results showed that compound 1 possessed the most potent effects with the IC50 values of 14.36 ± 1.04 μM against T24 cells. The further bioactivity analysis showed that compound 1 induced apoptosis of T24 cells, and altered anti- and pro-apoptotic proteins, leading to mitochondrial dysfunction and activation of caspase-3 for causing cell apoptosis. The present investigation illustrated compound 1 might be used as a potential antitumour chemotherapy candidate. 相似文献
89.
90.
Michel Weïwer Trevor Sherwood Robert J. Linhardt 《Journal of carbohydrate chemistry》2013,32(7):420-427
Floridoside (2-O-glycerol-α-D-galactopyranoside) is a natural glycerol glycoside found in red algae and is believed to play important roles in carbon storage, transport, and assimilation and in the regulation of osmotic balance. We describe here a rapid, high-yield, and high-stereoselectivity synthesis of floridoside in which the key step involves the 1,2-cis O-glycosylation of 1,3-dibenzylglycerol with ethyl 2,3,4,6-tetra-O-benzyl-1-thio-β-D-galactopyranoside using iodonium dicollidine perchlorate (IDCP) or N-iodosuccinimide/trimethylsilyl triflate (NIS/TMSOTf) as promoters. 相似文献