全文获取类型
收费全文 | 1819篇 |
免费 | 142篇 |
国内免费 | 1篇 |
专业分类
化学 | 1352篇 |
晶体学 | 6篇 |
力学 | 31篇 |
数学 | 215篇 |
物理学 | 358篇 |
出版年
2024年 | 1篇 |
2023年 | 18篇 |
2022年 | 16篇 |
2021年 | 75篇 |
2020年 | 73篇 |
2019年 | 106篇 |
2018年 | 102篇 |
2017年 | 77篇 |
2016年 | 127篇 |
2015年 | 92篇 |
2014年 | 97篇 |
2013年 | 135篇 |
2012年 | 133篇 |
2011年 | 162篇 |
2010年 | 95篇 |
2009年 | 70篇 |
2008年 | 108篇 |
2007年 | 101篇 |
2006年 | 106篇 |
2005年 | 82篇 |
2004年 | 58篇 |
2003年 | 44篇 |
2002年 | 34篇 |
2001年 | 6篇 |
2000年 | 9篇 |
1999年 | 5篇 |
1998年 | 3篇 |
1997年 | 4篇 |
1996年 | 5篇 |
1995年 | 5篇 |
1993年 | 3篇 |
1992年 | 5篇 |
1990年 | 1篇 |
1988年 | 1篇 |
1983年 | 1篇 |
1981年 | 1篇 |
1979年 | 1篇 |
排序方式: 共有1962条查询结果,搜索用时 31 毫秒
1.
Dmitry I. Bugaenko Alexey A. Volkov Dr. Mikhail V. Livantsov Prof. Dr. Marina A. Yurovskaya Dr. Alexander V. Karchava 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(54):12502-12506
The visible-light-induced arylation of tertiary phosphines with aryl(mesityl)iodonium triflates to produce the quaternary phosphonium salts occurs under mild, metal, and catalyst-free conditions. Photo-excited EDA complexes between diaryliodonium salts and phosphines supposedly enable this transformation, which is difficult to achieve through the traditional ground-state reactions. Demonstrating high functional group tolerance, broad scope, and complete selectivity of the aryl group transfer, the method is particularly compatible with sterically congested phosphines, which are challenging under metal-based catalytic methods. 相似文献
2.
Michael A. Pudovik Lyudmila Kibardina Alexey Trifonov Alexey Dobrynin Sergei Katsyuba Alexander Burilov 《Phosphorus, sulfur, and silicon and the related elements》2019,194(1-2):120-126
New O-phosphorylated pyridoxal derivatives have been synthesized through the reaction of azomethines with РV acid chlorides. 2-Chloro-2-thioxo-5,5-dimethyl-1,3,2-dioxaphosphinanes and diethylchlorothiophosphate have been employed as phosphorylating agents. Regardless of the nature of the phosphorylating agent, the reaction is regioselective at phenolic hydroxyl group. The structure of final products is determined by the nature of the substituent at the nitrogen atom. If R is alkyl or cycloalkyl group, the products of the reaction represent phosphorylated pyridoxal imines, whereas phosphorylated furopyridines are formed in the case R is aryl substituent. 相似文献
3.
4.
Bumagin Nikolay A. Petkevich Sergey K. Kletskov Alexey V. Alekseyev Roman S. Potkin Vladimir I. 《Chemistry of Heterocyclic Compounds》2019,55(6):508-516
Chemistry of Heterocyclic Compounds - N-(4,6-Dimethylpyrimidin-2-yl)-5-phenylisoxazole-3-carboxamide was used as a ligand for obtaining bimetallic boron-containing heterogeneous catalysts... 相似文献
5.
6.
Dr. Oliver Hegen Jens Braese Prof. Dr. Alexey Y. Timoshkin Prof. Dr. Manfred Scheer 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(2):485-489
A new class of neutral bidentate ligands with pnictogenyl-functional sites has been obtained. The reaction of tmeda⋅(BH2I)2 ( 1 , tmeda=tetramethylethylendiamine) with different phosphanides yields the corresponding bidentate phosphanylboranes tmeda⋅(BH2PH2)2 ( 2 a ), tmeda⋅(BH2PPh2)2 ( 2 b ), and tmeda⋅(BH2tBuPH)2 ( 2 c ). This reaction strategy could be further extended to synthesize the first bidentate arsanylborane tmeda⋅(BH2AsPh2)2 ( 3 ). Depending on the substituents on the phosphorus, these compounds form different AuI complexes, to build either polymeric tmeda⋅(BH2PH2AuCl)2 ( 4 a ), or monomeric tmeda⋅(BH2PPh2AuCl)2 ( 4 b ) products. These compounds form also neutral oligomeric group 13/15 chain-like molecules by coordination to a boron moiety such as tmeda⋅(BH2PH2BH3)2 ( 5 a ) and tmeda⋅(BH2AsPh2BH3)2 ( 5 b ). DFT calculations provide insight into the differences between the syntheses of mono- and bidentate pnictogenylboranes. 相似文献
7.
8.
9.
Copper Causes Regiospecific Formation of C4F8‐Containing Six‐Membered Rings and their Defluorination/Aromatization to C4F4‐Containing Rings in Triphenylene/1,4‐C4F8I2 Reactions 下载免费PDF全文
Kerry C. Rippy Dr. Eric V. Bukovsky Dr. Tyler T. Clikeman Dr. Yu‐Sheng Chen Dr. Gao‐Lei Hou Dr. Xue‐Bin Wang Dr. Alexey A. Popov Dr. Olga V. Boltalina Prof. Steven H. Strauss 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(3):874-877
The presence of Cu in reactions of triphenylene (TRPH) and 1,4‐C4F8I2 at 360 °C led to regiospecific substitution of TRPH ortho C(β) atoms to form C4F8‐containing rings, completely suppressing substitution on C(α) atoms. In addition, Cu caused selective reductive‐defluorination/aromatization (RD/A) to form C4F4‐containing aromatic rings. Without Cu, the reactions of TRPH and 1,4‐C4F8I2 were not regiospecific and no RD/A was observed. These results, supported by DFT calculations, are the first examples of Cu‐promoted 1) regiospecific perfluoroannulation, 2) preparative C?F activation, and 3) RD/A. HPLC‐purified products were characterized by X‐ray diffraction, low‐temperature PES, and 1H/19F NMR. 相似文献
10.