全文获取类型
收费全文 | 273篇 |
免费 | 13篇 |
国内免费 | 13篇 |
专业分类
化学 | 293篇 |
晶体学 | 2篇 |
综合类 | 1篇 |
物理学 | 3篇 |
出版年
2023年 | 2篇 |
2022年 | 4篇 |
2021年 | 4篇 |
2020年 | 9篇 |
2019年 | 4篇 |
2018年 | 6篇 |
2017年 | 3篇 |
2016年 | 3篇 |
2015年 | 5篇 |
2014年 | 13篇 |
2013年 | 33篇 |
2012年 | 15篇 |
2011年 | 18篇 |
2010年 | 9篇 |
2009年 | 9篇 |
2008年 | 10篇 |
2007年 | 20篇 |
2006年 | 18篇 |
2005年 | 22篇 |
2004年 | 15篇 |
2003年 | 18篇 |
2002年 | 6篇 |
2001年 | 3篇 |
2000年 | 5篇 |
1999年 | 7篇 |
1998年 | 11篇 |
1997年 | 3篇 |
1996年 | 7篇 |
1995年 | 3篇 |
1994年 | 2篇 |
1993年 | 4篇 |
1992年 | 3篇 |
1991年 | 1篇 |
1987年 | 1篇 |
1985年 | 1篇 |
1978年 | 1篇 |
1973年 | 1篇 |
排序方式: 共有299条查询结果,搜索用时 15 毫秒
1.
Kimihiko SatoTsutomu Kishimoto Minoru MorimotoHiroyuki Saimoto Yoshihiro Shigemasa 《Tetrahedron letters》2003,44(47):8623-8625
A simple method for the hydrolysis of acetals and ketals was accomplished in neutral water or aqueous media by hydrothermal treatment without using acidic reagents. The deacetalization reaction was effectively accelerated in the presence of calcium chloride. Because no acidic catalysts were employed, neutralization of the reaction mixture was not necessary after the reaction. This sequence was successfully applied to the hydrolysis of chitosan, a biodegradable polyaminosaccharide. 相似文献
2.
Titanium tetrachloride promoted reaction of silyl ketene acetals with epoxides, followed by acidic work-up, affords butanolides in moderate/good yields. With epihalohydrins the reaction is regioselective and occurs at the less substituted end of the epoxide; the γ-haloalkyl-γ-butanolides thus obtained can be further transformed into various products. 相似文献
3.
4.
Rogelio P. Frutos Isabelle Gallou Diana Reeves Yibo Xu Dhileepkumar Krishnamurthy Chris H. Senanayake 《Tetrahedron letters》2005,46(48):8369-8372
Expedient and practical new methodology for the synthesis of substituted imidazoles was developed to provide a rapid access to a variety of 2-substituted, 1,2-disubstituted and 1,2,4-trisubstituted imidazoles by the direct CuCl-mediated reaction of nitriles with α-amino acetals in an intermolecular as well as intramolecular fashion. 相似文献
5.
A facile one-step method has been developed for the synthesis of N-protected α-amino aldehyde acetals in moderate to good yields by three-component reaction of fluoroalkanesulfonyl azides, vinyl ethers and alcohol at 0 °C within 10 min. This practical synthetic method provides a convenient and expeditious access to N-per(poly)fluoroalkanesulfonyl α-amino aldehyde acetals. 相似文献
6.
GIAO/DFT evaluation of 13C NMR chemical shifts of selected acetals based on DFT optimized geometries
DFT/B3LYP calculations of the ground-state conformation of eight cyclic and acyclic acetals are presented and compared with experimental data. Results of single-point GIAO/DFT calculations at five different levels of theory show that isotropic shieldings need to be empirically scaled to achieve agreement with experimental chemical shifts. Statistical evaluation of data indicates that the most accurate prediction of 13C chemical shifts is achieved at the MPW1PW91/6-311G** level of theory. An empirical equation describing the relationship between delta values and shielding constants is postulated. This equation has been applied to the non-chair ground-state conformation of the six-membered acetonide and to the conformationally flexible benzodioxonine derivative. The agreement observed between the experimental and predicted chemical shifts shows that calculations at the MPW1PW91/6-311G** level of theory are adequate for addressing questions of conformation. 相似文献
7.
Gafarova Yu. T. Dekhtyar" E. F. Dekhtyar" T. F. Fatykhov A. A. Spirikhin L. V. Vostrikova O. S. Zlotskii S. S. Dokichev V. A. 《Russian Chemical Bulletin》2003,52(4):1003-1008
Under mild conditions, trialkylalanes (Et3Al and Bui
3Al) in chlorine-containing solvents (CH2Cl2 or ClCH2CH2Cl) react with cyclic acetals and orthoformates to form glycol monoethers and dialkylacetals, respectively, in high yields. The 1H NMR spectroscopic data demonstrate that CH2Cl2 or ClCH2CH2Cl interacts with Bui
3Al. 相似文献
8.
The adsorption and thermal decomposition of ketene on Si(l 11)-7 × 7 were investigated using various surface analysis techniques. When the surface was exposed to ketene at 120 K, two CO stretching modes at 220 and 273 meV appeared in HREELS, corresponding to two adsorbed ketene states. After the sample was annealed at ?250 K, the 273 and the 80 meV peaks vanished, indicating the disappearance of one of the adsorption states by partial desorption of the adsorbate. In a corresponding TPD measurement, a desorption peak for ketene species was noted at 220 K. Annealing the sample at 450 K caused the decomposition of the adsorbate, producing CHx and O adspecies. Further annealing of the surface at higher temperatures resulted in the breaking of the CH bond, the desorption of H and O species and the formation of Si carbide. The desorption of H at 800 K was confirmed by the appearance of the D2 (m/e = 4) TPD peak at that temperature when CD2CO was used instead of CH2CO. 相似文献
9.
Under fluoride activation, the vinyl fluorine of perfluoroketene dithioacetal may be substituted by silylated nucleophiles. Using silyl alkynes, a formal transition metal free sila-Sonogashira cross-coupling reaction occurred. The resulting enynes were hydrolyzed giving new polyfunctional trifluoromethyl building blocks. 相似文献
10.
W. Dölling K. Kischkies F. Heinemann H. Hartung 《Monatshefte für Chemie / Chemical Monthly》1993,124(6-7):707-719
Summary The new alkyl 2-(2-oxo-benzazoline-3-yl)-3-hydroxy dithiocrotonates and dithiocinnamates4 and the corresponding ketene dithioacetals2 and5 are obtained by dithiocarboxylation of the 3-acceptormethyl substituted benzazoline-2-ones1 or3. Alkylation at room temperature gives compounds4 whereas at higher alkylation temperature2 or5 are formed. The results of X-ray analyses performed for methyl 3-hydroxy-p-chloro-dithiocinnamate4d and of N-[1-(4-chloro-benzoyl)-2,2-bis(methylthio)-vinyl]-benzothiazoline-2-one5e are discussed. 相似文献