全文获取类型
收费全文 | 1373篇 |
免费 | 151篇 |
国内免费 | 183篇 |
专业分类
化学 | 1651篇 |
晶体学 | 9篇 |
力学 | 8篇 |
综合类 | 1篇 |
物理学 | 38篇 |
出版年
2024年 | 1篇 |
2023年 | 19篇 |
2022年 | 24篇 |
2021年 | 38篇 |
2020年 | 59篇 |
2019年 | 49篇 |
2018年 | 57篇 |
2017年 | 50篇 |
2016年 | 74篇 |
2015年 | 40篇 |
2014年 | 87篇 |
2013年 | 115篇 |
2012年 | 125篇 |
2011年 | 93篇 |
2010年 | 69篇 |
2009年 | 85篇 |
2008年 | 70篇 |
2007年 | 103篇 |
2006年 | 85篇 |
2005年 | 85篇 |
2004年 | 66篇 |
2003年 | 47篇 |
2002年 | 66篇 |
2001年 | 27篇 |
2000年 | 21篇 |
1999年 | 20篇 |
1998年 | 17篇 |
1997年 | 19篇 |
1996年 | 23篇 |
1995年 | 10篇 |
1994年 | 14篇 |
1993年 | 13篇 |
1992年 | 11篇 |
1991年 | 2篇 |
1990年 | 6篇 |
1989年 | 1篇 |
1988年 | 2篇 |
1987年 | 2篇 |
1986年 | 1篇 |
1985年 | 1篇 |
1984年 | 2篇 |
1982年 | 2篇 |
1981年 | 1篇 |
1980年 | 2篇 |
1979年 | 1篇 |
1978年 | 1篇 |
1973年 | 1篇 |
排序方式: 共有1707条查询结果,搜索用时 196 毫秒
101.
102.
103.
Surfactant (SDS)‐mediated cleavage of imines was achieved with acetic anhydride to the corresponding carbonyls (aldehydes and ketones) and acetanilides in water at 25–30°C with very good to excellent yields, thus contributing significantly to the green chemistry concept. 相似文献
104.
Sankareswaran Srimurugan Paulsamy Suresh Thirukkallam Kanthadai Varadarajan 《合成通讯》2013,43(15):2483-2490
A facile method for the synthesis of (2R,3R)‐1,4‐dimethoxy‐1,1,4,4‐tetrasubstituted‐2,3‐butanediols involving oxidative cleavage of benzylidene acetal as a key step is described. These sterically hindered diols unusually formed cyclic sulfites as the major product under methanesulfonylation reaction conditions. 相似文献
105.
合成并表征了2个不对称大环双核铜配合物[Cu2(L1)Cl2]·CH3CN(1)和[Cu2(L2)Br2]·CH3CN·H2O(2)。配合物与CT-DNA的作用通过紫外-可见光谱,粘度实验,圆二色谱和凝胶电泳实验进行了研究。紫外-可见光谱的结果表明配合物与DNA的结合常数分别为6.2×105和7.2×105,圆二色谱的实验表明配合物能与DNA较好的结合,粘度实验表明配合物与DNA的结合为非典型的插入模式,凝胶电泳实验显示配合物通过氧化机理对DNA有较强的切割活性。 相似文献
106.
Vyacheslav I. Supranovich Gennady I. Borodkin Aleksey Yu. Vorob’ev Vyacheslav G. Shubin 《Tetrahedron letters》2014
An unusual cleavage of the Cpy–Cpy bond in the reaction of 2,2′-bipyridine N,N′-diimine and its C-methyl substituted derivatives with acetylenes is described. The effect of the solvent on the yield of 7,7′-bipyrazolo[1,5-a]pyridine-2,2′,3,3′-tetracarboxylates and the products of cleavage of the Cpy–Cpy bond has been studied. The mechanism of the cleavage reaction is discussed on the basis of DFT calculations. 相似文献
107.
108.
Effect of Various Intercalators on the Fenton‐Type Oxidative Cleavage of Double‐Stranded DNA
下载免费PDF全文
![点击此处可从《化学:亚洲杂志》网站下载免费的PDF全文](/ch/ext_images/free.gif)
Hyeon Jeong Kim Giwoong Sung Gyeongwon Kim Jongjin Park Prof. Dr. Biao Jin Prof. Dr. Seog K. Kim 《化学:亚洲杂志》2014,9(5):1341-1348
The intensity of the linear dichroism (LD) in the absorption region of DNA (about 260 nm) decreased with time in the presence of [Fe(EDTA)]2+ (EDTA=ethylenediaminetetraacetic acid), H2O2, and ascorbate. The decrease in the LD signal indicated either an increase in flexibility, a shortening of the DNA stem, or both, owing to oxidative cleavage, and was best described by the difference between the two single‐exponential‐decay curves, thereby suggesting the involvement of two sequential first‐order reactions. The fast reaction was assigned to cleavage of one of two DNA strands, which increased the flexibility of the DNA. The slow reaction corresponded to cleavage at or near the first cleavage site, thereby shortening the DNA stem. The presence of an intercalator, including ethidium, propidium, 9‐aminoacridine, and proflavine, inhibited the first step of the cleavage reaction. One of the possible reasons for the observed inhibition might be a change in the DNA conformation near the intercalation site. Intercalation caused an unwinding and elongation of the DNA and resulted in changes in the location of the H atoms of the sugar moiety, which is known to be the main site at which hydroxyl radicals react. 相似文献
109.
110.
Lorenzo Di Terlizzi Prof. Stefano Protti Prof. Davide Ravelli Prof. Maurizio Fagnoni 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(26):e202200313
With the aim of generating new, thermally inaccessible diradicals, potentially able to induce a double-strand DNA cleavage, the photochemistry of a set of chloroaryl-substituted carboxylic acids in polar media was investigated. The photoheterolytic cleavage of the Ar−Cl bond occurred in each case to form the corresponding triplet phenyl cations. Under basic conditions, the photorelease of the chloride anion was accompanied by an intramolecular electron-transfer from the carboxylate group to the aromatic radical cationic site to give a diradical species. This latter intermediate could then undergo CO2 loss in a structure-dependent fashion, according to the stability of the resulting diradical, or abstract a hydrogen atom from the medium. In aqueous environment at physiological pH (pH=7.3), both a phenyl cation and a diradical chemistry was observed. The mechanistic scenario and the role of the various intermediates (aryl cations and diradicals) involved in the process was supported by computational analysis. 相似文献