全文获取类型
收费全文 | 761篇 |
免费 | 26篇 |
国内免费 | 6篇 |
专业分类
化学 | 529篇 |
晶体学 | 4篇 |
力学 | 15篇 |
数学 | 102篇 |
物理学 | 143篇 |
出版年
2023年 | 6篇 |
2022年 | 37篇 |
2021年 | 31篇 |
2020年 | 31篇 |
2019年 | 27篇 |
2018年 | 30篇 |
2017年 | 23篇 |
2016年 | 39篇 |
2015年 | 18篇 |
2014年 | 29篇 |
2013年 | 37篇 |
2012年 | 56篇 |
2011年 | 45篇 |
2010年 | 29篇 |
2009年 | 21篇 |
2008年 | 27篇 |
2007年 | 22篇 |
2006年 | 39篇 |
2005年 | 30篇 |
2004年 | 21篇 |
2003年 | 21篇 |
2002年 | 21篇 |
2001年 | 10篇 |
2000年 | 7篇 |
1999年 | 5篇 |
1997年 | 5篇 |
1996年 | 8篇 |
1995年 | 9篇 |
1994年 | 8篇 |
1993年 | 3篇 |
1992年 | 5篇 |
1991年 | 4篇 |
1990年 | 3篇 |
1988年 | 2篇 |
1987年 | 2篇 |
1986年 | 7篇 |
1985年 | 4篇 |
1984年 | 4篇 |
1983年 | 7篇 |
1982年 | 6篇 |
1981年 | 14篇 |
1980年 | 8篇 |
1979年 | 6篇 |
1978年 | 2篇 |
1977年 | 2篇 |
1976年 | 5篇 |
1975年 | 5篇 |
1974年 | 3篇 |
1972年 | 3篇 |
1970年 | 2篇 |
排序方式: 共有793条查询结果,搜索用时 15 毫秒
61.
Ngoc Vinh Huynh Thi Hoai Thu Nguyen Kim Phi Phung Nguyen Poul Erik Hansen 《Magnetic resonance in chemistry : MRC》2013,51(7):439-443
Tithonia tagetiflora Desv. (Asteraceae) is a widespread plant in Vietnam, and the species of Tithonia are known as plants containing many biologically active compounds. However, T. tagetiflora's chemical composition remains mostly unknown. Therefore, we now report the structural elucidation of two new sesquiterpene lactones, 8‐angeloyloxy‐2,14‐epoxygermacra‐4,10(1),11(13)‐trien‐6,12‐olide (1) and 6‐angeloyloxy‐1‐hydroxy‐3,4‐epoxygermacra‐9,11(13)‐dien‐8,12‐olide (2), together with three known compounds, including two norisoprenoids, (6S,9S)‐vomifoliol or (6R,9R)‐vomifoliol (3) and (6S,9S)‐roseoside (4), and one glutinane type triterpene, epi‐glutinol (5), from the leaves of T. tagetiflora. Their structures are established by 1D and 2D NMR spectroscopy, as well as ESI‐MS analysis and comparison with literature data. Copyright © 2013 John Wiley & Sons, Ltd. 相似文献
62.
Christine Bressy Minh Ngoc NGuyen Brigitte Tanguy Van Giang Ngo André Margaillan 《Polymer Degradation and Stability》2010,95(7):1260-9117
Polymers containing hydrolytically labile trialkylsilyl ester side groups were synthesised via a conventional and a controlled radical polymerization. The trialkylsilyl methacrylate monomer unit was chosen for its capacity to hydrolyse into basic, acid or sea water varying the hydrophilic character of the resulting polymer backbone with time. The hydrolysis or saponification reaction of the ester bond of the trialkylsilyl methacrylate was monitored through a 1H NMR study showing the formation of siloxane side-products. Several copolymers and polymer blends were prepared as matrixes for controlled erodible systems. Their capacity to hydrolyse was demonstrated through SEM investigations with selective dissolution of free films containing hydrolysable copolymers and PMMA blends. Well-defined random and diblock copolymers with methyl methacrylate were investigated to show the effect of the microstructure on the erosion properties of the corresponding coatings. Poly(methyl methacrylate-b-tert-butyldimethylsilyl methacrylate) diblock copolymers synthesised through the RAFT process showed a better control of the erosion with a constant erosion rate over a long-time service in sea water at pH = 8.2. In addition, experiments showed that the erosion rate could be modulated by varying the molar proportion of hydrolysable side groups onto the copolymer backbone and the weight amount of copolymers mixed with PMMA in toluene solution. 相似文献
63.
The monoterpene (−)-isopulegol (7) has been used as a starting material for the total synthesis in eight/nine steps of two sesquiterpenes which were recently isolated from the medicinal plant Fabiana imbricata. Use of this approach has shown that a structure proposed as 3,11-amorphadiene (3) should be revised to that of 4,11-cadinadiene (18) and confirmed the structure proposed for the natural product 4-amorphen-1 1-ol (1). 相似文献
64.
65.
Dr. Aurélien Adenot Dr. Lucile Anthore-Dalion Dr. Emmanuel Nicolas Jean-Claude Berthet Dr. Pierre Thuéry Dr. Thibault Cantat 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(72):18047-18053
An air-tolerant Cu-catalyzed sulfonylative Hiyama cross-coupling reaction enabling the formation of diaryl sulfones is described. Starting from aryl silanes, DABSO and aryliodides, the reaction tolerates a large variety of polar functional groups (amines, ketones, esters, aldehydes). Control experiments coupled with DFT calculations shed light on the mechanism, characterized by the formation of a Cu(I)-sulfinate intermediate via fast insertion of a SO2 molecule. 相似文献
66.
67.
Yuanyin Chen Fafu Yang Pierre Thuéry Martine Nierlich Jacques Vicens 《Journal of inclusion phenomena and macrocyclic chemistry》2002,42(3-4):261-263
The X-ray structure of the alreadypublished p-tert-butylcalix[6]-1,4-2,5-bis(crown-4)1 is reported. Extraction of solid ammoniumpicrate in chloroform-d indicates thecation to be located outside of the calixcrown andforming a 1:2 (metal-ligand) complex. 相似文献
68.
Ngoc Binh Vo Le Anh Nguyen Tung Lam Pham Duy Tien Doan Thanh Binh Nguyen Quoc Anh Ngo 《Tetrahedron letters》2017,58(25):2503-2506
A procedure to exclusively obtain 3′S-cyanoanhydrovinblastine 12 from two naturally occurring vinca-alkaloids (catharanthine and vindoline) in one step with good yield is described. Stereoselective reductions of 12, providing straightforward access to three new vinca-alkaloids, including two diastereomers 3′S-cyano-(4′R,5′-dihydro)-anhydrovinblastine and 3′S-cyano-(4′S,5′-dihydro)-anhydrovinblastine as well as (3′S-aminomethyl)-(4′S,5′-dihydro)-anhydrovinblastine in good yields is also reported. 相似文献
69.
70.
An oxacalix[2]arene[2]pyrimidine-bis(ZnII-porphyrin) conjugate was readily prepared via nucleophilic aromatic substitution of a phenolic AB3-Zn-porphyrin on the upper rim of a (1,3-alternate) 5,17-bis(methylsulfonyl)oxacalix[4]arene precursor. Efficient 1:1 complex formation between the ‘jaws’ bisporphyrin tweezer and fullerene C70 was evidenced by 1H NMR titrations (K = 3.0 × 104 M−1), while no detectable complexation could be observed with C60. On the other hand, an analogous oxacalix[4]arene-bis(Cu-corrole) conjugate did not show any measurable (C60 or C70) fullerene binding. 相似文献